ProMade Elbow - Drilling Guide for Dia.3.2mm Drill
by LIMACORPORATE S.p.A. EUDAMEDGUDID
Active
Ref 9CC0.14.001Model 80333902A040BL
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing GUDID | Number08033390337847 | Date11 Aug 2026 | StatusIn distribution |
| European Union | CE/MDR EUDAMED | Number80333902A040BL | Date5 Aug 2026 | StatusActive |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
- European Union
- United States
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls on record, checked 23 Oct 2026.
Specification
- Trade Name
- ProMade Elbow - Drilling Guide for Dia.3.2mm Drill EUDAMEDProMade Elbow GUDID
- Generic Name
- Surgical drill guide, reusable
- Model / Ref / Catalog
- 80333902A040BL, 9CC0.14.001
- Primary DI / UDI-DI
- 08033390337847
- Basic UDI-DI
- 80333902A040BL
- FDA Product Code
- LXH
- EMDN Code
- L0922 Orthopaedic surgery guides, reusable
- GMDN Term
- Surgical drill guide, reusable
- Device Class
- Class IIa EUDAMEDClass I GUDID
- Regulation Number
- 888.4540
- Market of Registration
- Italy
- Commercial Distribution
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Device Class | Class IIa | Class I |
Manufacturer details
- EUDAMED SRN
- IT-MF-000010690
Other devices from LIMACORPORATE S.p.A.
Properties
Other properties (20)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No
- Manufacturing Date: No