FlexiGRAFT®
- Primary DI
- 00889858124591
- Brand
- FlexiGRAFT®
- Company
- LIFENET HEALTH
- Model
- FKG108036
- Catalog number
- FKG
- Device description
- Kinetigraft
- Published
- 2015-09-24
- Public version status
- Update
- Distribution status
- Not in Commercial Distribution
- MRI safety
- Labeling does not contain MRI Safety Information
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| GAT | Suture, Nonabsorbable, Synthetic, Polyethylene | General, Plastic Surgery | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 00889858124591 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | UPC-A | EAN-13 |
|---|
| 00889858124591 | 00889858124591 | 889858124591 | 0889858124591 |
GMDN Terms
| Term | Definition |
|---|
| Tendon graft | A sterile tendon tissue, which may include a bone block, intended for transplantation that is harvested from a human donor. The tissue is intended to be used to replace or strengthen damaged tendon in any part of the human body. It may include non-tissue components (e.g. suture) to facilitate its implantation or function. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Device Size Text, specify | 0 | |
| Device Size Text, specify | 0 | |
| Outer Diameter | 10 | Millimeter |
Regulatory Flags
- DUNS number
- 121828156
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- true
- Kit
- false
- Combination product
- false
- Lot or batch
- false
- Serial number
- true
- Manufacturing date on label
- false
- Expiration date on label
- true
- Donation ID number
- false
- Contains natural rubber latex
- false
- No natural rubber latex
- false
- Sterilization required before use
- false
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| 10840277410068 | ProZip Knotless Implant | RIVERPOINT MEDICAL, LLC | GAT | 2026-01-06 |
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