Symmetry Duval 36-6055
by Aspen Surgical Products, Inc.
Ref 36-6055Model 34-7001
Symmetry Duval 36-6055 is a Class I device made by Aspen Surgical Products, Inc., registered in EUDAMED on 27 May 2026 (Basic UDI-DI 08401132ForcepYB) and listed in FDA GUDID since 16 Sep 2022 (UDI-DI 00887482010471), active as of 25 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number08401132ForcepYB 00887482010471 | Date27 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00887482010471 | Date16 Sep 2022 | StatusListed |
Official records
- EUDAMED public site 08401132ForcepYB
- AccessGUDID record 00887482010471
Across registries
- EUDAMED Basic UDI-DI 08401132ForcepYB registered 27 May 2026 Active
- FDA GUDID UDI-DI 00887482010471 listed 16 Sep 2022 Listed
Timeline
- Listed FDA GUDID 00887482010471
- Registered EUDAMED 08401132ForcepYB
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Symmetry ® EUDAMEDSymmetry Duval GUDID
- Generic name
- Dressing/utility forceps, tweezers-like, reusable
- Device name
- Classic® Allis Tissue Forceps 5X6 6"
- Model / Ref / Catalog
- 36-6055, 34-7001
- Primary DI / UDI-DI
- 00887482010471
- Basic UDI-DI
- 08401132ForcepYB
- FDA product code
- GEN
- EMDN code
- L031399 General surgery forceps, reusable - other
- GMDN term
- Dressing/utility forceps, tweezers-like, reusable
- Device class
- Class I
- Regulation number
- 878.4800
- EU registration type
- Standard device
- EU market of registration
- Germany
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
- Size
- Length — 8 Inch
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