8840762
Ref 8840.762Model 10000201110
8840762 (8840.762) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 1 Sep 2026 (Basic UDI-DI B-04055207021033) and listed in FDA GUDID since 9 Aug 2022 (UDI-DI 04055207021033), 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-04055207021033 04055207021033 | Date1 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207021033 | Date9 Aug 2022 | StatusListed |
Official records
- EUDAMED public site B-04055207021033
- AccessGUDID record 04055207021033
Across registries
- EUDAMED Basic UDI-DI B-04055207021033 registered 1 Sep 2026 Active
- FDA GUDID UDI-DI 04055207021033 listed 9 Aug 2022 Listed
Timeline
- Listed FDA GUDID 04055207021033
- Registered EUDAMED B-04055207021033
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Gastrointestinal endoscopic clip applier
- Device name
- Clip applicators
- Model / Ref / Catalog
- 10000201110, 8840.762, 8840762
- Description
- TEM CLIP APPLICATOR Ø 6MM WL 435MM TL 555mm, take-apart, reusable
- Primary DI / UDI-DI
- 04055207021033
- Basic UDI-DI
- B-04055207021033
- FDA product code
- GDO
- EMDN code
- L020802 Multiple applicators of clips for video surgery, reusable
- GMDN term
- Gastrointestinal endoscopic clip applier
- 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
- Outer Diameter — 6 MillimeterLength — 435 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10000201110 8840.762 | 8840762 |
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