Peracidin® Drum
Peracidin® Drum (081896) is a Class II device made by Angelini Pharma Inc., cleared under FDA 510(k) K962959 on 5 Jun 1998 and listed in FDA GUDID since 22 Mar 2024 (UDI-DI 00898021000419), active as of 22 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00898021000419 | Date22 Mar 2024 | StatusListed |
| United States | FDA 510(k)SESE | NumberK962959 | Date5 Jun 1998 | StatusActive |
Official records
- AccessGUDID record 00898021000419
- FDA 510(k) database K962959
Across registries
- FDA 510(k) K962959 decided 5 Jun 1998 Active
- FDA GUDID UDI-DI 00898021000419 listed 22 Mar 2024 Listed
Timeline
- Cleared FDA 510(k) K962959
- Listed FDA GUDID 00898021000419
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Peracidin®
- Generic name
- Organic peroxy acid device sterilant, single-use
- Model / Ref / Catalog
- Drum, 081896
- Primary DI / UDI-DI
- 00898021000419
- 510(k) Number
- FDA product code
- MED
- GMDN term
- Organic peroxy acid device sterilant, single-use
- Device class
- Class II
- Regulation number
- 880.6885
- GUDID distribution status
- In Commercial Distribution
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