Tregor® 36511STER
Tregor® 36511STER (83454081) is a Class II device made by Aston Medical, listed in FDA GUDID since 16 Sep 2015 (UDI-DI 03663703000509), registry data as of 23 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 | Number03663703000509 | Date16 Sep 2015 | StatusListed |
Official records
- AccessGUDID record 03663703000509
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Tregor®
- Generic name
- Acetabular shell
- Model / Ref / Catalog
- 36511STER, 83454081
- Primary DI / UDI-DI
- 03663703000509
- FDA product code
- MEH
- GMDN term
- Acetabular shell
- Device class
- Class II
- Regulation number
- 888.3353
- GUDID distribution status
- In Commercial Distribution
- Size
- Outer Diameter — 4.5 MillimeterLength — 40 Millimeter
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