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Columbia 13-14
EUDAMEDFDA UDIClass I (EU MDR)
Ref 237-238XSIModel Dental hand instrument, curette for the removal of the subgingival and supragingival calculus
Identity
- Trade Name
- Columbia 13-14 EUDAMEDLMDental FDA UDI
- Generic Name
- Periodontal curette FDA UDI
- Device Name
- Periodontal hand instrument EUDAMEDColumbia 13-14, Universal Curette, Periodontics FDA UDI
- Model / Reference
- Dental hand instrument, curette for the removal of the subgingival and supragingival calculus EUDAMED237-238XSI EUDAMEDFDA UDI
- Description
- Columbia 13-14, Universal Curette, Periodontics FDA UDI
Identifiers
- Primary DI / UDI-DI
- 06438311209913 EUDAMEDFDA UDI
- Basic UDI-DI
- B-06438311209913 EUDAMED6438311PERIO1r06S EUDAMED
- Direct Marketing DI
- 06438311209913 EUDAMED
- FDA Product Code
- DZN FDA UDI
- EMDN Code
- L159001 DENTAL AND PERIODONTAL CURETTES, REUSABLE EUDAMED
- GMDN Term
- Periodontal curette 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
Columbia 13-14 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-06438311209913 | Class I | Active |
| EUDAMED | European Union | CE/MDD | B-06438311209913 | 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 cf1e256b-e67d-4307-b5c8-229cc6cea20f 61 fields · synced Sep 17, 2026
- EUDAMED 00fa87e5-60fc-4435-b8c4-dee5f900e951 61 fields · synced May 19, 2026
- FDA UDI 7e0c96ac-aa2c-49d7-bef9-e5c5cb4ea85b 33 fields · synced May 30, 2026