Lsss RM04053
Ref IN631/1
Lsss RM04053 is a Class I device made by Lockdown Medical Ltd, registered in EUDAMED on 4 Nov 2026 (Basic UDI-DI 0506043360DRILLTAPSLEEVXS) and listed in FDA GUDID since 24 Jul 2020 (UDI-DI 05060433600807), active as of 7 Nov 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 | Number0506043360DRILLTAPSLEEVXS 05060433600807 | Date4 Nov 2026 | StatusActive |
| United States | GUDID listing GUDID | Number05060433600807 | Date24 Jul 2020 | StatusListed |
Official records
- EUDAMED public site 0506043360DRILLTAPSLEEVXS
- AccessGUDID record 05060433600807
Across registries
- EUDAMED Basic UDI-DI 0506043360DRILLTAPSLEEVXS registered 4 Nov 2026 Active
- FDA GUDID UDI-DI 05060433600807 listed 24 Jul 2020 Listed
Timeline
- Listed FDA GUDID 05060433600807
- Registered EUDAMED 0506043360DRILLTAPSLEEVXS
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Lsss
- Generic name
- Surgical drill guide, reusable
- Model / Ref / Catalog
- IN631/1 EUDAMEDRM04053 GUDID
- Primary DI / UDI-DI
- 05060433600807
- Basic UDI-DI
- 0506043360DRILLTAPSLEEVXS
- Direct marketing DI
- 05060433600807
- FDA product code
- MDM, FZX, LXI
- EMDN code
- L0999 Orthopaedic and traumatological surgery instruments, reusable - other
- GMDN term
- Surgical drill guide, reusable
- Device class
- Class I
- Regulation number
- 878.4800, 878.4820
- EU registration type
- Standard device
- EU market of registration
- Ireland
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | IN631/1 | RM04053 |
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