Oral/Maxillofacial Surgical Kit

Awarded Award Notice Posted

Solicitation number
FA5587-17-Q-0006
Agency
Air Forces Europe and Africa Air Force, Department of Defense
Awarded
to Stryker UK LIMITED
Set-aside
No set-aside

Opportunity facts

Contract number
FA558717P0011 Federal contract award
NAICS code
339113 Surgical Appliance and Supplies Manufacturing
PSC
Not on record
Place of performance
RAF Lakenheath Brandon, United Kingdom

Notice details come from SAM.gov. Updated .

Notice text

Added: Dec 06, 2016 10:27 am

The 48 MDG requires a brand name or equal surgical kit comparable/anatomical equivalent to the brand Stryker Universal CMF instrumentation/implants for use on the mid-face. The Stryker Universal CMF surgery kit consists of 129 different line items for oral/maxillofacial surgeries. The 129 items are included in Attachment 1 - Surgical Kit Items. Contractor shall supply the surgical kit, on-site support and FOB destination delivery. This contract shall include a one (1) year warranty against defects in material or workmanship. During the warranty period, manufacturer shall repair or replace parts or products defective in material or workmanship. Warranty, shipping and delivery FOB Destination shall be included in CLIN 0001.


The Stryker Universal CMF brand name or equal surgical kit shall have the following salient characteristics:


- Shall be FDA Approved/Certified
- Titanium or Titanium alloy screws/plates/implants
- Manufacturer shall have a minimum of 30 years' experience in manufacturing Oral Maxillofacial Surgery implants.
- Shall have On-site representative support available; locally based representative highly desired but not mandatory (within 50 miles of RAF Lakenheath, England)
- On-site representative support shall be available between 0600 - 1800 GMT/London time, Monday through Friday, according to 48 MDG's surgery schedule requirements.
- On-site representative shall have a minimum of 12 months' experience supporting Oral Maxillofacial Surgeries in theater.
- Companies may be subject to end-user/surgeon approval for patient safety purposes, and may require a hands-on evaluation/comparison.

Attachments

Files attached to this notice, newest first
File Type Posted
Attachment_1_-_Surgical_Kit_Items.pdf PDF
Combo_IAW_12.603.pdf PDF

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