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Traus Series

EUDAMEDFDA UDIFDA 510(k)

Class IIa (EU MDR)

Ref SIP10

by Saeshin Precision Co., Ltd.

Identity

Trade Name
TRAUS SERIES EUDAMED
TRAUS SIP10 FDA UDI
Generic Name
Dental power tool system, line-powered FDA UDI
Device Name
TRAUS SERIES EUDAMED
32:1 , non-optic XIP10+FUS10+CRB27XX+MBP10SX FDA UDI
Model / Reference
SIP10 EUDAMED
TRAUS SIP10 #2 FDA UDI
Description
32:1 , non-optic XIP10+FUS10+CRB27XX+MBP10SX FDA UDI

Identifiers

Primary DI / UDI-DI
08809260470712 EUDAMEDFDA UDI
Basic UDI-DI
B-08809260470712 EUDAMED
FDA Product Code
EKY FDA UDI
EMDN Code
L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Dental power tool system, line-powered 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

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

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

Traus Series by Saeshin Precision Co., Ltd. — Class IIa — FDA_510K, MDD — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (2 countries)

Regulatory Authorizations

United States Active

FDA_510K

European Union Active

CE/MDD

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Manufacturer

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

Sources (3)

  • EUDAMED 75010a18-0306-4a78-a36d-d3c3a04260fe 61 fields · synced Jun 19, 2026
  • FDA UDI 0747549e-ddb4-42c8-b5a1-9300bcd11531 33 fields · synced May 30, 2026
  • FDA 510(k) K123695 1 fields · synced May 18, 2026