Identity
- Trade Name
- creos™ syntoprotect FDA UDI
- Generic Name
- Pliable-polymer dental regeneration membrane, non-bioabsorbable FDA UDI
- Device Name
- creos™ syntoprotect Ti-reinforced PTFE membrane 250 No11 FDA UDI
- Model / Reference
- N1625TI-11-1 FDA UDI
- Description
- creos™ syntoprotect Ti-reinforced PTFE membrane 250 No11 FDA UDI
Identifiers
- Catalog Number
- N1625TI-11-1 FDA UDI
- Primary DI / UDI-DI
- 07332747181692 FDA UDI
- FDA Product Code
- LYC FDA UDI
- GMDN Term
- Pliable-polymer dental regeneration membrane, non-bioabsorbable FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 872.3930 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
MR Conditional FDA UDI
Dimensions & Sizes
- Size
- Height — 250.000 Micrometer FDA UDI
creos™ syntoprotect by Nobel Biocare AG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Nobel Biocare AG
Sources (1)
- FDA UDI af138ce7-ae93-437d-af2c-deeae500fdb6 38 fields · synced Jun 6, 2026