JAZZ System
Listed
Valid until
Not applicable
FDA recalls
None foundDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03607505503356 | Date25 May 2016 | StatusListed |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Surgical implant/trial-implant/sizer holder, reusable
- Model / Ref / Catalog
- JAZZ CLAW - Implant Holder Hook / Blocker, 550335
- Primary DI / UDI-DI
- 03607505503356
- FDA Product Code
- OWI
- GMDN Term
- Surgical implant/trial-implant/sizer holder, reusable
- Device Class
- Class II
- Regulation Number
- 888.3010
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Implanet
Properties
Other properties (13)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No