ArTT 9055.34.113
Part of a family of 53 devices: see the family page
Ref 9055.34.113Model 80333902A005BJ
ArTT 9055.34.113 is a device classified as Class IIa in the EU and Class I in the US made by Limacorporate, registered in EUDAMED on 29 Oct 2026 (Basic UDI-DI 80333902A005BJ) and listed in FDA GUDID since 25 Sep 2025 (UDI-DI 08033390304870), 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 | Number80333902A005BJ 08033390304870 | Date29 Oct 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08033390304870 | Date25 Sep 2025 | StatusListed |
Official records
- EUDAMED public site 80333902A005BJ
- AccessGUDID record 08033390304870
Across registries
- EUDAMED Basic UDI-DI 80333902A005BJ registered 29 Oct 2026 Active
- FDA GUDID UDI-DI 08033390304870 listed 25 Sep 2025 Listed
Timeline
- Listed FDA GUDID 08033390304870
- Registered EUDAMED 80333902A005BJ
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- General Instrument - Long Drill Bit Dia.4,5mm/L.60mm EUDAMEDArTT GUDID
- Generic name
- Fluted surgical drill bit, reusable
- Model / Ref / Catalog
- 9055.34.113, 80333902A005BJ
- Primary DI / UDI-DI
- 08033390304870
- Basic UDI-DI
- 80333902A005BJ
- FDA product code
- HWE
- EMDN code
- L091199 Orthopaedic prosthetics instruments, reusable - other
- GMDN term
- Fluted surgical drill bit, reusable
- Device class
- Class IIa EUDAMEDClass I GUDID
- Regulation number
- 878.4820
- EU registration type
- Standard device
- EU market of registration
- Italy
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device class | Class IIa | Class I |
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