Penlon 408001015
by Penlon, Ltd.
Penlon 408001015 is a Class I device made by Penlon, Ltd., listed in FDA GUDID since 6 Dec 2024 (UDI-DI 05051977003711), not in commercial distribution (GUDID) as of 23 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 | Number05051977003711 | Date6 Dec 2024 | StatusListed |
Official records
- AccessGUDID record 05051977003711
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Penlon
- Generic name
- Laryngoscope blade, reusable
- Model / Ref / Catalog
- 408001015
- Primary DI / UDI-DI
- 05051977003711
- FDA product code
- CCW
- GMDN term
- Laryngoscope blade, reusable
- Device class
- Class I
- Regulation number
- 868.5540
- GUDID distribution status
- Not in Commercial Distribution
- MRI safety
- MR Safe
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