Saturday, 18 March 2017

Medical Device Contract Manufacturing — RK Manufacturing Corporation


RK has two operational groups: Medical Device Contract Manufacturingand Machine Tool Development and Manufacture. We have the knowledge and experience to take your product / design from inception to final packaging. Our certified quality inspectors monitor every process, so you can be sure your product will be defect free. We have the capability and capacity to assist you in completing all of your assembly needs.
At RK Manufacturing, we pride ourselves on having the best customer service in the industry. Our knowledgeable staff is always ready to assist you. Quick response time and attention to quality make us an invaluable supplier to our customers. Our flexible manufacturing capabilities allow us to produce large and small quantities quickly and cost efficiently.
  • Design and Development Assistance
  • Prototyping
  • Custom Manufacturing
  • Short lead times
  • Orders sizes from 1 to 1,000,000
  • Complete suture and medical device assembly
  • Clean room/White room environments
  • Final sterilization of packaged product
  • Full lot control and traceability
  • Sterilization validation and processing
  • Validation protocol development, testing and reports
  • Complete work order history
  • Worldwide shipping
The Machine Tool Development and Manufacturing Group offers:
  • Tooling, fixture design and fabrication
  • Prototyping
  • Precision machined suture processing equipment
  • Comprehensive Machining services
  • Worldwide shipping

Originally published at rkmcorp.com.

RKM Products -Medical device contract manufacturing


As a contract manufacturer RK Manufacturing produces customer’s products to their design specifications. Non Disclosure Agreement’s typically govern the information that can be shared with potential customers. RKM currently manufactures, assembles, and packages specialty sutures. The current sutures range in size from #7–0 to #5 and are assembled with many of the standard suture materials in the market and several proprietary ones. The suture materials are either monofilament or braided configurations. The sutures are either individually packaged or loaded in bulk.
RK also assembles devices that contain surgical screws and ferrules.

Originally published at rkmcorp.com.

Thursday, 2 March 2017

Medical device contract manufacturing- RKMCorp


As a contract manufacturer RK Manufacturing produces customer’s products to their design specifications. Non Disclosure Agreement’s typically govern the information that can be shared with potential customers. RKM currently manufactures, assembles, and packages specialty sutures. The current sutures range in size from #7–0 to #5 and are assembled with many of the standard suture materials in the market and several proprietary ones. The suture materials are either monofilament or braided configurations. The sutures are either individually packaged or loaded in bulk.
RK also assembles devices that contain surgical screws and ferrules.

Saturday, 18 February 2017

Contract Manufacturing — RK Manufacturing (Medical device contract manufacturing)


We offer full machine shop services to our customers, including custom made fixtures, tooling, dies and equipment, to help transform your ideas into finished product.
Our machine shop services include:
  • CNC milling and turning for machined components
  • Precision custom tooling
  • Separate final packing rooms
  • Prototype machining services
  • Heat treating, grinding, welding and assembly
  • Design assistance
  • In-house tool and die
RK is capable of contracting to produce medical devices that require manufacture, assembly, testing, and packaging in a clean room environment. We have certified sterilization sub-contractors to bring your product to operating room levels of sterilization. Our Quality Management System has been certified to ISO 9001 and ISO 13485 to assure you of quality products made by Current Good Manufacturing Practices (CGMP).

Originally published at rkmcorp.com.

Tuesday, 14 February 2017

Figure 8 Winder - RK Manufacturing Medical Manufacturing Companies


The Automatic Figure 8 Winder is used to wind the suture into the suture card in a figure 8 shape for easy dispensing.
The suture card is placed into the nest, with left hand. The un-needled end of the suture is placed between the feed rolls using the thumb and forefinger of the right hand and is fed automatically into the suture card forming a figure 8 shape. The needle will stop once it reaches your fingers. The needle is then slid out of the feed rolls and inserted into the suture card.
Notes:
  • The feed rolls feed the suture into the suture card using very little tension, so not to damage the suture material or cause injury to fingers by needle.

Originally published at rkmcorp.com.

Sunday, 29 January 2017

Medical device contract manufacturing (Rack Winder) - RK Manufacturing



An easy way to prepare braided suture material
The RK Rack Winder is used to prepare braided suture material for needle attaching. The suture ends are tipped (stiffened) so they can be easily inserted into the needles and sutures are cut to their required length.

Size: 48″ wide x 42″ deep — Workspace: 80″ x 80″ — Yield: 2,000/hour

The braided suture material is wound from a spool on to a rack, approximately 200 sutures/rack. The circumference of the rack determines suture length. The speed of the rack is adjustable, at 65 rpm (recommended speed); a rack of 200 sutures would take approximately three minutes.

Read more- Medical device manufacturing

After the rack is wound, it is removed and placed on a table, where a medical grade cyanoacrylate adhesive is applied to a two inch (or as required) portion of the sutures. The adhesive is applied by hand using a small piece of foam and cures in three minutes.
After the adhesive has cured, the suture rack is place into the suture-cutting fixture as shown. The sutures are held in position and cut from the rack using a hand held rotary knife. The sutures are cut through the two inch tipped portion leaving a one inch tipped length at the end of each suture.

Notes:
It is recommended to have three racks for each required suture length. This would allow one rack to be wound, while adhesive is applied to another and sutures are cut from the third rack. Using three racks the operator should yield approximately 2,000 tipped sutures per hour. The racks are not adjustable and are made per your specific suture length requirements.

Read more- Medical Manufacturing Companies
Originally published at rkmcorp.com.

Friday, 20 January 2017

RKM Quality — RK Manufacturing(Medical device contract manufacturing)


Quality Policy
R.K. Manufacturing Corp. is committed to providing quality products and services to the medical device industry that exceeds the expectations and needs of our customers. We are committed to complying with regulatory requirements and maintaining the effectiveness of our quality management system.
Our Mission
R.K. Manufacturing Corporation’s mission is to provide its customers with consistently high quality and to provide a competitive edge to support our customer’s positions in the health care market.
Quality Values and Beliefs
  • Outstanding service to our Customers
  • Innovation, quality, and value in our products
  • Respect for our customers, suppliers, employees and community
  • Creativity and teamwork in the workplace
  • Honesty and integrity in all that we do
Regulatory
  • Registered by BSI for ISO 13485 Medical Device Manufacturing
  • Registered by BSI for ISO 9001Quality Management Systems
  • FDA Registered Manufacturing facility, Registration number # 1226146
  • Compliant with Medical Device Directive (MDD) 2007
  • Compliant with 21CFR Part 820, (current Good Manufacturing Practice)

Read more- Medical Manufacturing Companies

Originally published at rkmcorp.com.

Thursday, 12 January 2017

Product Catalog-RK Manufacturing

Drilled — End Needle Attaching Machines
The attaching machines can be purchased separately or as a complete machine.





RK Mono Winder
The RK Mono Winder is used to cut monofilament sutures from a spool to their required length.








RK Rack Winder
The RK Rack Winder is used to prepare braided suture material for needle attaching.









Automatic Figure 8 Suture Winder
The Automatic Figure 8 Winder is used to wind the suture into the suture card in a figure 8 . shape for easy dispensing 

Friday, 6 January 2017

Clean Rooms - RKM Corp

A Clean room is an enclosed area within a building with a controlled environment where products are manufactured, assembled or packaged. It is a room in which the concentration of airborne particles is controlled to specified limits. Clean rooms are classified according to the number and size of particles permitted per volume of air. Large numbers like “class 100” or “class 1000” refer to FED-STD-209E, and denote the number of particles of size 0.5 µm or larger permitted per cubic foot of air. Small numbers refer to ISO 14644-1 standards, which specify the decimal logarithm of the number of particles 0.1 µm or larger permitted per cubic meter of air. Both FS 209E and ISO 14644-1 assume log-log relationships between particle size and particle concentration. For that reason, there is no such thing as zero particle concentration. US FED STD 209E was officially canceled by the General Services Administration of the US Department of Commerce November 29, 2001, but is still widely used.
Eliminating sub-micron airborne contamination in a clean room is really a process of control. People, process, facilities and equipment generate air born contaminants. They must be continually removed from the air. The only way to control contamination is to control the total environment. Air flow rates and direction, pressurization, temperature, humidity and specialized filtration all need to be employed and tightly controlled. Whenever possible the sources of these particles need to be controlled or eliminated. There is more to a clean room than air filters. Clean rooms are planned and manufactured using strict protocol and methods. They are frequently found in electronics, pharmaceutical, biopharmaceutical, medical device industries and other critical manufacturing environments. Once a Clean room is built it must be maintained and cleaned to the same high standards.
Contamination is a process or act that causes materials or surfaces to be soiled with contaminating substances. There are two broad categories of surface contaminants: film type and particulates. A partial list of contaminants is found below. Preventing these contaminants from entering the Clean room environment is the objective. Strict procedures should be followed whenever entering or cleaning a Clean room.
Facilities
  • Walls, floors and ceilings
  • Paint and coatings
  • Construction material (sheet rock, saw dust etc.)
  • Air conditioning debris
  • Room air and vapors
  • Spills and leaks
People
  • Skin flakes and oil
  • Cosmetics and perfume
  • Spittle
  • Clothing debris (lint, fibers etc.)
  • Hair
Tool Generated
  • Friction and wear particles
  • Lubricants and emissions
  • Vibrations
  • Brooms, mops and dusters
Fluids
  • Particulates floating in air
  • Bacteria, organics and moisture
  • Floor finishes or coatings
  • Cleaning chemicals
  • Plasticizers (outgases)
  • Deionized water
Product Generated
  • Nylon, Polyester, Metal chips
  • Quartz flakes
  • Clean room debris
  • Aluminum particles
Contaminate Control is addressed through:
Clean room Design – Clean rooms are designed to achieve and maintain a airflow in which essentially the entire body of air within a confined area moves with uniform velocity along parallel flow lines. This air flow is called laminar flow. The more restriction of air flow the more turbulence. Turbulence can cause particle movement.
HEPA (High Efficiency Particulate Air Filter) – These filters are extremely important for maintaining contamination control. They filter particles as small as 0.3 microns with a 99.97% minimum particle-collective efficiency.
Filtration – In addition to the HEPA filters commonly used in Clean rooms, there are a number of other filtration mechanisms used to remove particles from gases and liquids. These filters are essential for providing effective contamination control.
Cleaning- Cleaning is an essential element of contamination control. Applications and procedures need to be written and agreed upon by Clean room management and contractors (if used).
Clean room Garments – The requirements for Clean room garments will vary from location to location. It is important to know the local garment requirements of the Clean room management. Gloves, face masks and head covers are standard in nearly every Clean room environment. Smocks are being used more and more. Jump suits are required in very clean environments.
Worker Behavior – There are both physical and psychological concerns when humans are present in clean rooms. Physical behavior like fast motion and horseplay, sneezing and coughing can increase contamination. The body’s regenerative processes: skin flakes, oils, perspiration and hair are sources of contamination. Psychological concerns like room temperature, humidity, claustrophobia, odors and workplace attitude are topics to be addressed in the use of a clean room.
Commodities – Care must be taken when selecting and using commodity items in clean rooms. Wipers, clean room paper and pencils and other supplies that service the clean room should be carefully screened and selected. Review of the local clean room requirements for approving and taking these items into the clean room are essential.
Cosmetics – Many cosmetics contain sodium, magnesium, silicon, calcium, potassium or iron. These chemicals can create damaging particles. Clean room managers may ban or restrict cosmetics in the clean room.
Measurement and Instruments – Some important measurements related to contamination control are particle count, air flow & velocity, humidity, temperature and surface cleanliness. Specific standards should be set, and instruments to measure these factors should be utilized
Electrostatic Discharge (ESD) – When two surfaces rub together an electrical charge can be created. Moving air creates a charge. People touching surfaces or walking across the floor can create a turboelectric charge. Special care may need to be taken to use ESD protective materials to prevent damage from ESD.
Some typical general regulations recommended as a minimum for the successful operation of a clean room are:
  • No eating, smoking or gum chewing allowed inside the clean room.
  • Only garments approved for the clean room should be worn when entering.
  • All personal items such as keys, watches, rings, matches, lighters and cigarettes should be stored in the personal locker outside the gowning room.
  • Valuable personal Items such as wallets may be permitted in the clean room provided they are NEVER removed from beneath the clean room garments.
  • No cosmetics shall be worn in the clean rooms. This includes: rouge, lipstick, eye shadow, eyebrow pencil, mascara, eye liner, false eye lashes, fingernail polish, hair spray, mousse, or the heavy use of aerosols, after shaves and perfumes.
  • Use of paper or fabric towels are prohibited
  • Approved ball point pens shall be the only writing tool used.
  • Only approved clean room paper shall be allowed in the clean room.
  • Gloves or finger cots should not be allowed to touch any item or surface that has not been thoroughly cleaned.
  • Only approved gloves, finger cots (powder-free), pliers, tweezers should be used to handle product. Finger prints can be a major source of contamination on some products.
  • Solvent contact with the bare skin should be avoided. They can remove skin oils and increase skin flaking.
  • Approved skin lotions or lanolin based soaps are sometimes allowed. These can reduce skin flaking.
  • All tools, containers and fixtures used in the cleaning process should be cleaned to the same degree as the clean room surfaces. All of these items are a source of contamination.
  • No tool should be allowed to rest on the surface of a bench or table. It should be placed on a clean room wiper.
  • Only clean room approved wipers are allowed to be used. The wipers must be approved for the Class of clean room.
  • All equipment, materials and containers introduced into a sterile facility must be subjected to stringent sterilization prior to entrance.
  • No one who is physically ill, especially with respiratory or stomach disorders, may enter a sterile room. This is a good practice in any clean room environment.

Monday, 2 January 2017

Medical Device Contract Manufacturing — RK Manufacturing Corporation

RK has two operational groups: Medical Device Contract Manufacturing
and Machine Tool Development and Manufacture. We have the knowledge and experience to take your product/design from inception to final packaging. Our certified quality inspectors monitor every process, so you can be sure your product will be defect free. We have the capability and capacity to assist you in completing all of your assembly needs.

At RK Manufacturing, we pride ourselves on having the best customer service in the industry. Our knowledgeable staff is always ready to assist you. Quick response time and attention to quality make us an invaluable supplier to our customers. Our flexible manufacturing capabilities allow us to produce large and small quantities quickly and cost efficiently.
The Medical Device Contract Manufacturing Group offers:
Design and Development Assistance
Prototyping
Custom Manufacturing
Short lead times
Orders sizes from 1 to 1,000,000
Complete suture and medical device assembly
Clean room/White room environments
Final sterilization of packaged product
Full lot control and traceability
Sterilization validation and processing
Validation protocol development, testing and reports
Complete work order history
Worldwide shipping

The Machine Tool Development and Manufacturing Group offers:
Tooling, fixture design and fabrication
Prototyping
Precision machined suture processing equipment
Comprehensive Machining services
Worldwide shipping

Originally published at rkmcorp.com.