Na BIOD5S-Al-252-Rt
by Sterilmed, Inc. United States GUDID
Product code NLH
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10888551006262 | Date22 Sep 2016 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-0555-2009
SteriMed, Inc is conducting a product removal of a small group of devices individually packaged and sealed within a pouch. The removal is being conducted because the possibility exists that some of the pouches were not properly sealed on one end. A breach in packaging seal or a failure in packaging integrity has the possibility of risk to the patient in terms of transmitting organisms capable
Specification
- Trade Name
- Na
- Generic Name
- Cardiac mapping catheter, percutaneous, reprocessed
- Model / Ref / Catalog
- BIOD5S-AL-252-RT
- Primary DI / UDI-DI
- 10888551006262
- 510(k) Number
- FDA Product Code
- NLH
- GMDN Term
- Cardiac mapping catheter, percutaneous, reprocessed
- Device Class
- Class II
- Regulation Number
- 870.1220
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Ethylene Oxide
Other devices from Sterilmed, Inc.
Properties & raw data
Show properties, registry sources and raw records
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
Sources (1)
- FDA UDI 99f98dc2-036f-4fdd-be6d-c1bee69f7f22