Tissu-Trans Filtron 250cc
by Shippert Medical Technologies Corp.
Listed
Valid until
Not applicable
FDA recalls
None ongoingDocuments
None
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00893398002172 | Date10 Aug 2016 | StatusListed |
Recalls
-
- Completed Z-1335-2019
- Completed Z-1330-2019
- Completed Z-1336-2019
- Completed Z-1331-2019
- Completed Z-1332-2019
The pouch integrity of the sterile product can't be assured without a visual examination due to possibly containing a cut or hole in the pouch.
-
- Completed Z-1334-2019
- Completed Z-1333-2019
-
- Terminated Z-0170-2018
Potential breach of sterility of the packaging.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade Name
- Tissu-Trans Filtron
- Generic Name
- Surgical suction system collection container, single-use
- Model / Ref / Catalog
- Tissu-Trans Filtron 250cc, 3-TT-FILTRON 250
- Primary DI / UDI-DI
- 00893398002172
- 510(k) Number
- FDA Product Code
- MUU
- GMDN Term
- Surgical suction system collection container, single-use
- Device Class
- Class II
- Regulation Number
- 878.5040
- GUDID distribution status
- Not in Commercial Distribution
Other devices from Shippert Medical Technologies Corp.
Properties
Other properties (9)
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Serial Number: No
- Manufacturing Date: No