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Sickle LM23
EUDAMEDFDA UDIClass I (EU MDR)
Ref 313-314XSIModel Dental hand instrument, sickle scaler for the removal of the supragingival calculus
Identity
- Trade Name
- Sickle LM23 EUDAMEDLMDental FDA UDI
- Generic Name
- Manual dental scaler, reusable FDA UDI
- Device Name
- Periodontal hand instrument EUDAMEDSickle LM23, Scaler, Periodontics FDA UDI
- Model / Reference
- Dental hand instrument, sickle scaler for the removal of the supragingival calculus EUDAMED313-314XSI EUDAMEDFDA UDI
- Description
- Sickle LM23, Scaler, Periodontics FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06438311213071 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06438311213071 EUDAMED6438311PERIO1r06S EUDAMED
- Direct Marketing DI
- 06438311213071 EUDAMED
- FDA Product Code
- DZN FDA UDI
- EMDN Code
- L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
- GMDN Term
- Manual dental scaler, 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
Sickle LM23 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-06438311213071 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-06438311213071 | 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 50f691bb-b8e8-4694-a075-9ed2c22db950 61 fields · synced Jul 11, 2026
- EUDAMED 7ba88d58-90a4-4ded-b9a4-2e268346a269 61 fields · synced May 19, 2026
- FDA UDI 8f886b75-53eb-406a-80ec-1c64a120f1cd 33 fields · synced May 26, 2026