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Air Motor & Air Handpiece & Coupling

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref CAB10LN

by Saeshin Precision Co., Ltd.

Identity

Trade Name
AIR MOTOR & AIR HANDPIECE & COUPLING EUDAMED
TRAUS Air Dental Handpiece FDA UDI
Generic Name
Dental surgical power tool motorized handpiece/set, pneumatic FDA UDI
Device Name
AIR MOTOR & AIR HANDPIECE & COUPLING EUDAMED
TRAUS CAB10LN FDA UDI
Model / Reference
CAB10LN EUDAMED
TRAUS CAB10LN #1 FDA UDI
Description
TRAUS CAB10LN FDA UDI

Identifiers

Primary DI / UDI-DI
08809260473010 EUDAMEDFDA UDI
Basic UDI-DI
B-08809260473010 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 EUDAMED
Class 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Electrical-only medical device connection cable, reusable

Air Motor & Air Handpiece & Coupling by Saeshin Precision Co., Ltd. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrical-only medical device connection cable, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
KR-MF-000016345
Authorised Representative
Meridius Medical Europe Limited IE-AR-000004258

Sources (2)

  • EUDAMED 5c7b7b9e-763f-4ac1-a7cf-7b2156cd9bcc 61 fields · synced Jul 17, 2026
  • FDA UDI a693d636-4068-498e-b626-e80b7f5fdd92 34 fields · synced May 30, 2026