BiMobile Dual Mobility System - Instruments 184-352/56
by WALDEMAR LINK GmbH & Co. KG
Listed
Valid until
Not applicable
FDA recalls
1 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04026575279586 | Date25 Jan 2023 | StatusListed |
Recalls
-
- Ongoing Z-1219-2024
Mislabeled: Packaging incorrectly reflects a MobileLink Dual Mobility insert type F when it should reference G may cause a delay in surgery
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- BiMobile Dual Mobility System - Instruments
- Generic Name
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Model / Reference
- 184-352/56
- Primary DI / UDI-DI
- 04026575279586
- 510(k) Number
- FDA Product Code
- LZO, MEH
- GMDN Term
- Orthopaedic prosthesis implantation positioning instrument, reusable
- Device Class
- Class II
- Regulation Number
- 888.3353
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from WALDEMAR LINK GmbH & Co. KG
Properties
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No