Hex Driver for Ratchet DRHDES125
Ref DRHDES125Model DENTIS Implant Surgical Instrument System
Active
CE MDR
Valid until
Not listed
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR EUDAMED | Number88061691DENTIS-I7L 08806169139238 | Date27 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08806169139238 | Date1 Jun 2021 | StatusListed |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade Name
- Hex Driver for Ratchet
- Generic Name
- Surgical screwdriver, reusable
- Device Name
- DENTIS Implant Surgical Instrument System
- Model / Reference
- DRHDES125, DENTIS Implant Surgical Instrument System
- Primary DI / UDI-DI
- 08806169139238
- Basic UDI-DI
- 88061691DENTIS-I7L
- FDA Product Code
- NDP
- EMDN Code
- P01020180 Dental implants - accessories
- GMDN Term
- Surgical screwdriver, reusable
- Device Class
- Class I
- Regulation Number
- 872.3980
- Market of Registration
- Spain
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Other devices from Dentis Co., Ltd
Properties
Other properties (20)
- Sterile: No
- Single Use: No
- Implantable: No
- Reusable: 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