Landanger I050334-45
by Landanger
Ref I050334-45Model SURGICAL CANNULAS, ASPIRATION AND IRRIGATION MODELS, REUSABLE
Landanger I050334-45 is a Class I device made by Landanger, registered in EUDAMED on 16 Oct 2026 (Basic UDI-DI B-03661219468363) and listed in FDA GUDID since 22 Jan 2026 (UDI-DI 03661219468363), active as of 23 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-03661219468363 03661219468363 | Date16 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number03661219468363 | Date22 Jan 2026 | StatusListed |
Official records
- EUDAMED public site B-03661219468363
- AccessGUDID record 03661219468363
Across registries
- EUDAMED Basic UDI-DI B-03661219468363 registered 16 Oct 2026 Active
- FDA GUDID UDI-DI 03661219468363 listed 22 Jan 2026 Listed
Timeline
- Listed FDA GUDID 03661219468363
- Registered EUDAMED B-03661219468363
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Landanger
- Generic name
- Surgical irrigation/aspiration cannula, non-illuminating, reusable
- Model / reference
- I050334-45, SURGICAL CANNULAS, ASPIRATION AND IRRIGATION MODELS, REUSABLE
- Primary DI / UDI-DI
- 03661219468363
- Basic UDI-DI
- B-03661219468363
- FDA product code
- LRP
- EMDN code
- L030101 Suction and irrigation surgical cannulas and handpieces, reusable
- GMDN term
- Surgical irrigation/aspiration cannula, non-illuminating, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- France
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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