8379732
Ref 8379.732Model 10000277704
8379732 (8379.732) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 5 Oct 2026 (Basic UDI-DI B-04055207041901) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207041901), 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-04055207041901 04055207041901 | Date5 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207041901 | Date9 Aug 2022 | StatusListed |
Official records
- EUDAMED public site B-04055207041901
- AccessGUDID record 04055207041901
Across registries
- EUDAMED Basic UDI-DI B-04055207041901 registered 5 Oct 2026 Active
- FDA GUDID UDI-DI 04055207041901 listed 9 Aug 2022 Listed
Timeline
- Listed FDA GUDID 04055207041901
- Registered EUDAMED B-04055207041901
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- General-purpose endoscopic needle, reusable
- Device name
- Reusable cannulas
- Model / Ref / Catalog
- 10000277704, 8379.732, 8379732
- Description
- CANNULA FOR INJECTION Ø 3MM WL 340MM tip Ø 1.4mm, with Luer connection, reusable
- Primary DI / UDI-DI
- 04055207041901
- Basic UDI-DI
- B-04055207041901
- FDA product code
- GEA
- EMDN code
- L1207 Laparoscopic and thoracoscopic surgery cannulas, reusable
- GMDN term
- General-purpose endoscopic needle, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 340 MillimeterOuter Diameter — 3 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10000277704 8379.732 | 8379732 |
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