Permatage 5cc OS-PER-1001
by Abyrx, Inc.
Permatage 5cc OS-PER-1001 is a device classified as Unclassified made by Abyrx, Inc., listed in FDA GUDID since 24 Oct 2023 (UDI-DI 00850391007238), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00850391007238 | Date24 Oct 2023 | StatusListed |
Official records
- AccessGUDID record 00850391007238
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Permatage 5cc
- Generic name
- Bone wax, synthetic
- Model / reference
- OS-PER-1001
- Primary DI / UDI-DI
- 00850391007238
- FDA product code
- MTJ
- GMDN term
- Bone wax, synthetic
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Safe
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