SteriPack Group

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Contact: Linda Gilsenan - Sales & Marketing Executive
Web: http://www.steripackgroup.com
E-Mail:
Address: Kilbeggan Road, Clara, Ireland
Phone: +353-(57)-9331888 | Fax: +353-(57)-9331887 | Map/Directions >>

Profile: SteriPack Group is a supplier of cleanroom sterilized packaging solutions for the medical device industry. We can supply customized top web printed rolls for use on the automatic packing machines. The print and repeat length can be adjusted to fit the exact needs. Our meticulously calibrated measuring systems can maintain the exact repeat lengths to meet with any machine requirements. For base web we can supply PA/PE, PE/PA/PE, EVA/Surlyn/EVA, polyolefin and polypropylene monofilm structures which are suitable for form fill & sealing applications. Headerbags are a robust alternative to pouches for larger products. Our collection includes a breathable strip of coated Tyvek® which allows gas to penetrate, enabling easy access for bulky products. We offer materials suitable for wound care packaging in roll stock or pouch format to suit the packaging operation. We can also arrange to fully pack and sterilize the product ready for market as part of our contract packaging service.

The company is ISO 9001:2008, 13485:2003 certified.

FDA Registration Number: 3009217531
US Agent: Mona Manahi
Phone: +1-(212)-367-7274 Fax: +1-(212)-826-9509 E-Mail:

20 Products/Services (Click for related suppliers)

• Calcium Compound Bone Void Filler (FDA Code: MQV / 888.3045)

A resorbable calcium salt bone void filler device is a resorbable implant intended to fill bony voids or gaps of the extremities, spine, and pelvis that are caused by trauma or surgery and are not intrinsic to the stability of the bony structure.

• Cemented Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: JDI / 888.3350)

A hip joint metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and an acetabular resurfacing component made of ultra-high molecular weight polyethylene and is limited to those prostheses intended for use with bone cement (888.3027).

• Cleanroom Assembly and Packagings

• Contract Manufacturers

• Contract Manufacturing

• Contract Packaging

• Durable Product Contract Manufacturing

• Intramedullary Fixation Rod and Accessories (FDA Code: HSB / 888.3020)

An intramedullary fixation rod is a device intended to be implanted that consists of a rod made of alloys such as cobalt-chromium-molybdenum and stainless steel. It is inserted into the medullary (bone marrow) canal of long bones for the fixation of fractures.

• Medical Device Contract Manufacturing

• Medical Device Packaging Services

• Medical Packaging Services

• Medical Packagings

• Metal/Polymer Semi-Constrained Hip Prosthesis (FDA Code: LPH / 888.3358)

A hip joint metal/polymer/metal semi-constrained porous-coated uncemented prosthesis is a device intended to be implanted to replace a hip joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across the joint. This generic type of device has a femoral component made of a cobalt-chromium-molybdenum (Co-Cr-Mo) alloy or a titanium-aluminum-vanadium (Ti-6Al-4V) alloy and an acetabular component composed of an ultra-high molecular weight polyethylene articulating bearing surface fixed in a metal shell made of Co-Cr-Mo or Ti-6Al-4V. The femoral stem and acetabular shell have a porous coating made of, in the case of Co-Cr-Mo substrates, beads of the same alloy, and in the case of Ti-6Al-4V substrates, fibers of commercially pure titanium or Ti-6Al-4V alloy. The porous coating has a volume porosity between 30 and 70 percent, an average pore size between 100 and 1,000 microns, interconnecting porosity, and a porous coating thickness between 500 and 1,500 microns. The generic type of device has a design to achieve biological fixation to bone without the use of bone cement.

• Packaging

• Packaging and Sterilization Services

• Piston Syringe (FDA Code: FMF / 880.5860)

A piston syringe is a device intended for medical purposes that consists of a calibrated hollow barrel and a movable plunger. At one end of the barrel there is a male connector (nozzle) for fitting the female connector (hub) of a hypodermic single lumen needle. The device is used to inject fluids into, or withdraw fluids from, the body.

• Rollstock For Packaging

• Semi-Constrained Patellofemorotibial Knee Prosthesis (FDA Code: JWH / 888.3560)

A knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis is a device intended to be implanted to replace a knee joint. The device limits translation and rotation in one or more planes via the geometry of its articulating surfaces. It has no linkage across-the-joint. This generic type of device includes prostheses that have a femoral component made of alloys, such as cobalt-chromium-molybdenum, and a tibial component or components and a retropatellar resurfacing component made of ultra-high molecular weight polyethylene. This generic type of device is limited to those prostheses intended for use with bone cement (888.3027).

• Sterilization Packaging

• Syringe Holder Adapter (FDA Code: IQG / 890.5050)

A daily activity assist device is a modified adaptor or utensil (e.g., a dressing, grooming, recreational activity, transfer, eating, or homemaking aid) that is intended for medical purposes to assist a patient to perform a specific function.