Landanger O611822
by Landanger
Landanger O611822 is a Class I device made by Landanger, listed in FDA GUDID since 23 Sep 2022 (UDI-DI 03661219327905), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03661219327905 | Date23 Sep 2022 | StatusListed |
Official records
- AccessGUDID record 03661219327905
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Landanger
- Generic name
- Sterilization container mat
- Model / reference
- O611822
- Primary DI / UDI-DI
- 03661219327905
- FDA product code
- LRP
- GMDN term
- Sterilization container mat
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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