V. Mueller BP32VS
Listed
Valid until
Not applicable
FDA recalls
2 ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00724995233686 | Date10 Aug 2026 | StatusListed |
Recalls
-
- Ongoing Z-1236-2023
Product did not meet shelf-life testing requirements resulting in a breach of the sterility of the Genesis container holding surgical equipment.
-
- Ongoing Z-0203-2023
Genesis STERRAD Reusable Rigid Sterilization Containers have not consistently met the requirements for aerosol challenge testing.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- V. Mueller
- Generic Name
- Device sterilization/disinfection container, reusable
- Model / Ref / Catalog
- BP32VS
- Primary DI / UDI-DI
- 00724995233686
- 510(k) Number
- FDA Product Code
- KCT
- GMDN Term
- Device sterilization/disinfection container, reusable
- Device Class
- Class II
- Regulation Number
- 880.6850
- GUDID distribution status
- In Commercial Distribution
Other devices from Steris Corporation
Properties
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No