Acufex 72203429
Acufex 72203429 is a Class I device made by Smith & Nephew, Inc., listed in FDA GUDID since 29 Aug 2015 (UDI-DI 00885554026870), 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 | Number00885554026870 | Date29 Aug 2015 | StatusListed |
Official records
- AccessGUDID record 00885554026870
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Acufex
- Generic name
- Ligament reconstruction instrument set, reusable
- Model / Ref / Catalog
- 72203429
- Description
- ACUFEX PINPOINT DOUBLE-BUNDLE BULLET SUPPORT 6-7MM
- Primary DI / UDI-DI
- 00885554026870
- FDA product code
- NBH
- GMDN term
- Ligament reconstruction instrument set, reusable
- Device class
- Class I
- Regulation number
- 888.1100
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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