LM-LiftOut S5
Ref 812250Model Hand instrument for tooth extraction
Active
CE MDD
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/MDD EUDAMED | NumberB-06438311220765 06438311220765 | Date8 Dec 2021 | StatusActive |
| United States | GUDID listing GUDID | Number06438311220765 | Date31 Aug 2020 | 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- Withdrawn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
- LM-LiftOut S5 EUDAMEDLMDental GUDID
- Generic Name
- Dental elevator, tooth/root
- Model / Reference
- Hand instrument for tooth extraction, 812250
- Primary DI / UDI-DI
- 06438311220765
- Basic UDI-DI
- B-06438311220765
- FDA Product Code
- EMJ
- EMDN Code
- L150301 Dental extraction tooth forceps, reusable
- GMDN Term
- Dental elevator, tooth/root
- Device Class
- Class I
- Regulation Number
- 872.4565
- EU market of registration
- Finland
- GUDID distribution status
- In Commercial Distribution
- Sterilization Method
- Moist Heat or Steam Sterilization
Manufacturer details
- EUDAMED SRN
- FI-MF-000006705
Other devices from LM-Instruments Oy
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
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Serial Number: No
- Expiration Date: No