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Root Tip Pick DTS U
EUDAMEDFDA UDIClass I (EU MDR)
Ref 769-771ESTUModel Dental hand instrument, instrument for the removal of root tip
Identity
- Trade Name
- Root Tip Pick DTS U EUDAMEDLMDental FDA UDI
- Generic Name
- Dental elevator, tooth/root FDA UDI
- Device Name
- Root Tip Pick DTS U, Extraction FDA UDI
- Model / Reference
- Dental hand instrument, instrument for the removal of root tip EUDAMED769-771ESTU EUDAMEDFDA UDI
- Description
- Root Tip Pick DTS U, Extraction FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06438311057712 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06438311057712 EUDAMED
- FDA Product Code
- DZN FDA UDI
- EMDN Code
- L150301 DENTAL EXTRACTION TOOTH FORCEPS, REUSABLE EUDAMED
- GMDN Term
- Dental elevator, tooth/root FDA UDI
Classification
- Device Class
- Class I EUDAMEDFDA UDI
- Regulation Number
- 872.4565 FDA UDI
- Market of Registration
- Finland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Root Tip Pick DTS U by LM-Instruments Oy — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-06438311057712 | Class I | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- LM-Instruments Oy
- EUDAMED SRN
- FI-MF-000006705
Sources (2)
- EUDAMED 5e94852f-8c62-432a-89c7-b58c3c4a5bd9 61 fields · synced Jun 20, 2026
- FDA UDI a58d5859-fa68-4313-ad39-1351fc38ae47 33 fields · synced May 30, 2026