Symmetry Lemmon 55-7041
by Aspen Surgical Products, Inc.
Part of a family of 58 devices: see the family page
Ref 55-7041
Symmetry Lemmon 55-7041 is a Class I device made by Aspen Surgical Products, Inc., registered in EUDAMED on 15 Jul 2026 (Basic UDI-DI 08401132DissectorZW) and listed in FDA GUDID since 22 Sep 2022 (UDI-DI 00887482085462), active as of 24 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 | Number08401132DissectorZW 00887482085462 | Date15 Jul 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00887482085462 | Date22 Sep 2022 | StatusListed |
Official records
- EUDAMED public site 08401132DissectorZW
- AccessGUDID record 00887482085462
Across registries
- EUDAMED Basic UDI-DI 08401132DissectorZW registered 15 Jul 2026 Active
- FDA GUDID UDI-DI 00887482085462 listed 22 Sep 2022 Listed
Timeline
- Listed FDA GUDID 00887482085462
- Registered EUDAMED 08401132DissectorZW
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Symmetry ® EUDAMEDSymmetry Lemmon GUDID
- Generic name
- Open-surgery dissector
- Device name
- Dissectors (resuable)
- Model / Ref / Catalog
- 55-7041
- Primary DI / UDI-DI
- 00887482085462
- Basic UDI-DI
- 08401132DissectorZW
- Direct marketing DI
- 00887482085462
- FDA product code
- GDI
- EMDN code
- L0315 General surgery dissectors, reusable
- GMDN term
- Open-surgery dissector
- 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 — 6.375 Inch
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