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Root Canal Excavator 2.0mm
EUDAMEDFDA UDIClass I (EU MDR)
Ref 652-662ESModel Dental hand instrument, excavator for preparation of root canal
Identity
- Trade Name
- Root Canal Excavator 2.0mm EUDAMEDLMDental FDA UDI
- Generic Name
- Dental excavator, reusable FDA UDI
- Device Name
- Endodontic hand instruments Ir EUDAMEDRoot Canal Excavator 2.0mm, Endodontics FDA UDI
- Model / Reference
- Dental hand instrument, excavator for preparation of root canal EUDAMED652-662ES EUDAMEDFDA UDI
- Description
- Root Canal Excavator 2.0mm, Endodontics FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06438311218076 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06438311218076 EUDAMED6438311ENDO1r0SD EUDAMED
- Direct Marketing DI
- 06438311218076 EUDAMED
- FDA Product Code
- DZN FDA UDI
- EMDN Code
- L159002 DENTAL EXCAVATORS, REUSABLE EUDAMED
- GMDN Term
- Dental excavator, reusable 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 Canal Excavator 2.0mm by LM-Instruments Oy — Class I — MDR, MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | B-06438311218076 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-06438311218076 | 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 (3)
- EUDAMED 804074d5-4343-4472-bf08-36ae5a037d07 61 fields · synced Jul 13, 2026
- EUDAMED 2d590c4a-c9ec-44fc-bed3-e0cac73bfa80 61 fields · synced May 19, 2026
- FDA UDI 00d55133-6c91-49a4-8198-4e58fd0ec28f 33 fields · synced May 30, 2026