8393515
Ref 8393.515Model 10000201264
8393515 (8393.515) is a Class I device made by Richard Wolf GmbH, registered in EUDAMED on 7 Sep 2026 (Basic UDI-DI B-04055207016169) and listed in FDA GUDID since 12 Dec 2022 (UDI-DI 04055207016169), 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-04055207016169 04055207016169 | Date7 Sep 2026 | StatusActive |
| United States | GUDID listing GUDID | Number04055207016169 | Date12 Dec 2022 | StatusListed |
Official records
- EUDAMED public site B-04055207016169
- AccessGUDID record 04055207016169
Across registries
- EUDAMED Basic UDI-DI B-04055207016169 registered 7 Sep 2026 Active
- FDA GUDID UDI-DI 04055207016169 listed 12 Dec 2022 Listed
Timeline
- Listed FDA GUDID 04055207016169
- Registered EUDAMED B-04055207016169
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Generic name
- Suturing needle holder, reusable
- Device name
- Mod. needle holder inserts with sheath
- Model / Ref / Catalog
- 10000201264, 8393.515, 8393515
- Description
- NEEDLE HOLDER INSERT WITH SHEATH Ø 5MM curved left with carbide insert, WL 320mm, with irrigation connection, reusable
- Primary DI / UDI-DI
- 04055207016169
- Basic UDI-DI
- B-04055207016169
- FDA product code
- FHQ
- EMDN code
- L1205 Laparoscopic and thoracoscopic surgery needle holders, reusable
- GMDN term
- Suturing needle holder, reusable
- Device class
- Class I
- Regulation number
- 876.4730
- 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 — 5 Millimeter
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 10000201264 8393.515 | 8393515 |
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