creos™ syntoprotect
- Primary DI
- 07332747181753
- Brand
- creos™ syntoprotect
- Company
- Nobel Biocare AB
- Model
- N1615TI-04-1
- Catalog number
- N1615TI-04-1
- Device description
- creos™ syntoprotect Ti-reinforced PTFE membrane 150 No4
- Published
- 2021-01-13
- Public version status
- New
- Distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
- Rx
- true
- OTC
- false
- Sterile
- true
- Single use
- true
Product Codes
| Code | Name |
|---|
| LYC | Bone grafting material, synthetic |
Product Code Classifications
| Code | Device | Specialty | Class |
|---|
| LYC | Bone Grafting Material, Synthetic | Dental | 2 |
Identifiers And Packaging
| Identifier | Type | Agency | Package quantity | Status |
|---|
| 07332747181753 | Primary | GS1 | 0 | |
Alternate GTIN / UPC / EAN Codes
| Source identifier | GTIN-14 normalized | EAN-13 |
|---|
| 07332747181753 | 07332747181753 | 7332747181753 |
GMDN Terms
| Term | Definition |
|---|
| Pliable-polymer dental regeneration membrane, non-bioabsorbable | A sterile non-bioabsorbable material intended to be used to aid in the regeneration of tooth support, lost due to periodontal disease or trauma, by acting as a barrier to prevent the down-growth of soft tissue (connective tissue and epithelial cells) into the underlying bone during the healing period. It is a pliable synthetic polymer material that is held in place between soft tissue and bone [e.g., with ligatures, sutures, or pins (may be attached/included)] and applied during periodontal flap surgery and other guided bone regeneration (GBR) and guided tissue regeneration (GTR) surgical procedures. A plasticizer to soften the membrane may be included. This is a single-use device. |
Device Sizes
| Type | Value | Unit |
|---|
| Height | 150 | Micrometer |
Storage And Handling
| Type | Low | High | Condition |
|---|
| Special Storage Condition, Specify | 0 | 0 | Lower limit of temperature * 15°C. Upper limit of temperature * 30°C |
| Storage Environment Temperature | 15 Degrees Celsius | 30 Degrees Celsius | |
Regulatory Flags
- DUNS number
- 353939929
- Device count
- 1
- DM exempt
- false
- Premarket exempt
- false
- HCT/P
- false
- Kit
- false
- Combination product
- false
- Lot or batch
- true
- Serial number
- false
- 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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