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Air Motor & Air Handpiece & Coupling
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref CAB10LK
Identity
- Trade Name
- AIR MOTOR & AIR HANDPIECE & COUPLING EUDAMEDTRAUS Air Dental Handpiece FDA UDI
- Generic Name
- Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
- Device Name
- AIR MOTOR & AIR HANDPIECE & COUPLING EUDAMEDTRAUS CAB10LK FDA UDI
- Model / Reference
- CAB10LK EUDAMEDTRAUS CAB10LK #1 FDA UDI
- Description
- TRAUS CAB10LK FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08809260473027 EUDAMEDFDA UDI
- Basic UDI-DI
- B-08809260473027 EUDAMED
- 510(k) Number
- K221741 FDA UDI
- FDA Product Code
- EFB FDA UDI
- EMDN Code
- L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
- GMDN Term
- Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass I FDA UDI
- Regulation Number
- 872.4200 FDA UDI
- Market of Registration
- Belgium 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
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Air Motor & Air Handpiece & Coupling by Saeshin Precision Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-08809260473027 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Saeshin Precision Co., Ltd.
- EUDAMED SRN
- KR-MF-000016345
- Authorised Representative
- Meridius Medical Europe Limited IE-AR-000004258
Sources (2)
- EUDAMED 05e984d0-1987-4959-8591-d7ad58ae0c8f 61 fields · synced Jul 15, 2026
- FDA UDI cb624723-fe1c-4c41-9788-6cd70782b374 34 fields · synced May 30, 2026