BIATAIN Alginate Ag
by Advanced Medical Solutions Limited 4 variants
BIATAIN Alginate Ag (375559980) is a device classified as Unclassified made by Advanced Medical Solutions Limited, cleared under FDA 510(k) K090453 on 26 Feb 2009 and listed in FDA GUDID since 7 Dec 2022 (UDI-DI 05032749034430), active as of 22 Oct 2026. 3 FDA recalls are linked to it.
Active
Valid until
No expiry
FDA recalls
2 ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number05032749034430 | Date7 Dec 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK090453 | Date26 Feb 2009 | StatusActive |
Official records
- AccessGUDID record 05032749034430
- FDA 510(k) database K090453
Across registries
- FDA 510(k) K090453 decided 26 Feb 2009 Active
- FDA GUDID UDI-DI 05032749034430 listed 7 Dec 2022 Listed
Recalls
-
- Ongoing Z-1806-2022
- Ongoing Z-1805-2022
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. This device with this specific storage temperature deviation is not likely to cause adverse health consequences.
-
- Terminated Z-2719-2016
On 08 January 2015 AMS Sole Customer for the products notified AMS of the issue after discovering the misplaced IFUs during its review of packaging in its warehouse
Timeline
- Cleared FDA 510(k) K090453
- Recall initiated FDA recalls Z-2719-2016
- Recall initiated FDA recalls Z-1806-2022
- Recall initiated FDA recalls Z-1805-2022
- Listed FDA GUDID 05032749034430
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Biatain
- Generic name
- Exudate-absorbent dressing, hydrophilic-gel, antimicrobial
- Model / Ref / Catalog
- Alginate Ag, 375559980
- Primary DI / UDI-DI
- 05032749034430
- 510(k) Number
- FDA product code
- FRO
- GMDN term
- Exudate-absorbent dressing, hydrophilic-gel, antimicrobial
- Device class
- U
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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