Fisherbrand SCMF
by Fisher Scientific Company L.L.C.
Active
510(k)
Valid until
No expiry
FDA recalls
1 ongoingDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00613647000038 | Date24 Sep 2016 | StatusListed |
| United States | FDA 510(k)SESE | NumberK941327 | Date22 Dec 1994 | StatusActive |
Recalls
-
- Ongoing Z-1791-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Fisherbrand
- Generic name
- Sterilization packaging, single-use
- Model / Ref / Catalog
- SCMF, 0181254
- Primary DI / UDI-DI
- 00613647000038
- 510(k) Number
- FDA product code
- KCT
- GMDN term
- Sterilization packaging, single-use
- Device class
- Class II
- Regulation number
- 880.6850
- GUDID distribution status
- In Commercial Distribution
Other devices from Fisher Scientific Company L.L.C.
Properties
Other properties (10)
- Supplied sterile: No
- Sterilise before 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