BIOFOAM
- Primary DI
- 00889797015202
- Brand
- BIOFOAM
- Company
- WRIGHT MEDICAL TECHNOLOGY, INC.
- Model
- 46641022
- Catalog number
- 46641022
- Device description
- Wedge Trial
- Published
- 2016-09-17
- Public version status
- Update
- Distribution status
- In Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- false
- Single use
- false
Product Codes
| Code | Name |
|---|
| HWC | Screw, fixation, bone |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| HWC | Screw, Fixation, Bone | Orthopedic | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00889797015202 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00889797015202 | 00889797015202 | 889797015202 | 0889797015202 |
GMDN Terms
| Term | Definition |
|---|
| Surgical implant template, reusable | A device designed to determine the appropriate size and placement of a non-dental implant for a patient prior to or during implantation surgery. It is typically available as a graduated set or an individual plate (e.g., a translucent plastic sheet or a cut metal shape) with patterns/sizes corresponding to the size of the implant to be used to aid the surgeon in final selection of implant size, placement, and/or adaption. It is used for, e.g., total- or partial-joint prostheses, bone fracture fixation implants (plates, nails, including skull plate implants) or other types of surgical implants. This is a reusable device. |
Device Sizes
| Type | Value | Unit |
|---|
| Device Size Text, specify | 0 | |
Sterilization Methods
| Method |
|---|
| Moist Heat or Steam Sterilization |
Regulatory Flags
- DUNS number
- 807201207
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- true
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- Manufacturing date on label
- true
- Expiration date on label
- false
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- true
Other Devices From This Company
Other Devices Sharing Product Codes
| Primary DI | Brand | Company | Product code | Published |
|---|
| 00810211040227 | Headed Screw Partially Threaded Short 3.0mm,30mm Length | Pace Surgical, Inc. | HWC | 2026-03-19 |
| 08059386744369 | RONDO' | CITIEFFE SRL | HWC | 2026-03-17 |
| 00888867529038 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529083 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529090 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529113 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529144 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529151 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529182 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529212 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529373 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529434 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529441 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867529526 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867531918 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867531932 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867531949 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867531963 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867531970 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867531987 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867532007 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867532069 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867532083 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867532137 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867532144 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 00888867532281 | Arthrex® | ARTHREX, INC. | HWC | 2026-03-16 |
| 04053613298315 | Guide Pin Smooth | Gebr. Brasseler GmbH & Co. KG | HWC | 2026-03-11 |
| 00840124525474 | PolyLock Midfoot | FUSION ORTHOPEDICS, LLC | HWC | 2026-03-10 |
| 00840124525481 | PolyLock Midfoot | FUSION ORTHOPEDICS, LLC | HWC | 2026-03-10 |
| 00841506141442 | Distal Elbow Plating System | SKELETAL DYNAMICS L.L.C. | HWC | 2026-03-05 |