Identity
- Trade Name
- Permatage 5cc FDA UDI
- Generic Name
- Bone wax, synthetic FDA UDI
- Model / Reference
- OS-PER-1001 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00850391007238 FDA UDI
- FDA Product Code
- MTJ FDA UDI
- GMDN Term
- Bone wax, synthetic FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
Yes
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 Safe FDA UDI
Category: Bone wax, synthetic
Permatage 5cc by Abyrx, Inc. — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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- Ostene — Apatech Ltd · U
- Ostene — Apatech Ltd · U
- Abyrx Spatula — ABYRX, INC. · U
- AHBP 2.5 gram — ABYRX, INC. · U
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 U | Pending data |
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Manufacturer
- Manufacturer
- Abyrx, Inc.
Sources (1)
- FDA UDI 157230a9-f027-4359-ba27-e1aeda4f4143 32 fields · synced Jun 8, 2026