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Hoe Scaler, anterior DTS U
EUDAMEDFDA UDIClass I (EU MDR)
Ref 112-113ESTUModel Dental hand instrument, hoe scaler for the removal of the subgingival and supragingival calculus
Identity
- Trade Name
- Hoe Scaler, anterior DTS U EUDAMEDLMDental FDA UDI
- Generic Name
- Periodontal hoe FDA UDI
- Device Name
- Periodontal hand instrument EUDAMEDHoe Scaler, anterior DTS U, Periodontics FDA UDI
- Model / Reference
- Dental hand instrument, hoe scaler for the removal of the subgingival and supragingival calculus EUDAMED112-113ESTU EUDAMEDFDA UDI
- Description
- Hoe Scaler, anterior DTS U, Periodontics FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06438311021805 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06438311021805 EUDAMED6438311PERIO1r06S EUDAMED
- Direct Marketing DI
- 06438311021805 EUDAMED
- FDA Product Code
- DZN FDA UDI
- EMDN Code
- L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
- GMDN Term
- Periodontal hoe 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
Hoe Scaler, anterior DTS U 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-06438311021805 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-06438311021805 | 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 f25fa1d6-60ca-492f-8841-e2832b7acab5 61 fields · synced Jul 30, 2026
- EUDAMED 290bce8b-9001-4867-b0d5-49a9410fbce8 61 fields · synced May 19, 2026
- FDA UDI 1e919fa4-7556-4675-b705-d0521b7d7b91 33 fields · synced May 30, 2026