CC-Hook Right 202-1413
CC-Hook Right 202-1413 is a Class I device made by Xiros Ltd, listed in FDA GUDID since 25 Apr 2024 (UDI-DI 05060267134028), 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 | Number05060267134028 | Date25 Apr 2024 | StatusListed |
Official records
- AccessGUDID record 05060267134028
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- CC-Hook Right
- Generic name
- Suturing unit, single-use
- Model / Ref / Catalog
- 202-1413
- Primary DI / UDI-DI
- 05060267134028
- FDA product code
- GDG
- GMDN term
- Suturing unit, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
Similar devices in this category
Other devices filed under Suturing unit, single-use.
- OmniClose trocar site closure device FCL215000 by UNIMAX MEDICAL SYSTEMS INC.
- CONMED 9892 by Conmed Corporation
- EZPass™ 904051 by Biomet Orthopedics, Inc.
- EZPass™ 904052 by Biomet Orthopedics, Inc.
- Endo Close 173022 by Covidien LP
- CONMED 9893 by Conmed Corporation
- Green Genie Suture Passer 710001 by Aspen Surgical Products, Inc.
- Hoffee Suture Retriever 710000NS by Aspen Surgical Products, Inc.
- WECK IPN917216 EFX002 by TELEFLEX INCORPORATED
- 228143 by DePuy Mitek, Inc.