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TripleAngled BA Excavator2.0mm DTS
EUDAMEDFDA UDIClass I (EU MDR)
Ref 651-661ESTModel Dental hand instrument, excavator for the removal of softened carious dentin
Identity
- Trade Name
- TripleAngled BA Excavator2.0mm DTS EUDAMEDTripleAngled BA Excavator2.0mmDTS EUDAMEDLMDental FDA UDI
- Generic Name
- Dental excavator, reusable FDA UDI
- Device Name
- Restorative hand instrument Ir EUDAMEDTripleAngled BA Excavator 2.0mm DTS, Restoration FDA UDI
- Model / Reference
- Dental hand instrument, excavator for the removal of softened carious dentin EUDAMED651-661EST EUDAMEDFDA UDI
- Description
- TripleAngled BA Excavator 2.0mm DTS, Restoration FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06438311036366 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06438311036366 EUDAMED6438311RESTO1r0C6 EUDAMED
- Direct Marketing DI
- 06438311036366 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
TripleAngled BA Excavator2.0mm DTS 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-06438311036366 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-06438311036366 | 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 d19ee5cd-5b5a-4f93-ba8c-dcd9e9ca7bf4 61 fields · synced Jul 8, 2026
- EUDAMED 17e670b9-7104-4437-9d9f-ed46f0ede75e 61 fields · synced May 18, 2026
- FDA UDI c71db604-5566-4d53-8bcd-0eb69c75a6f4 33 fields · synced May 30, 2026