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Ultrasonic Surgical Series

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref SUS20

by Saeshin Precision Co., Ltd.

Identity

Trade Name
Ultrasonic Surgical Series EUDAMED
TRAUS SUS20 FDA UDI
Generic Name
Dental power tool system, line-powered FDA UDI
Device Name
Ultrasonic Sergical Series EUDAMED
non-optic / BUS20+FUS10+PEZ10XX FDA UDI
Model / Reference
SUS20 EUDAMED
TRAUS SUS20#2 FDA UDI
Description
non-optic / BUS20+FUS10+PEZ10XX FDA UDI

Identifiers

Primary DI / UDI-DI
08809260472150 EUDAMEDFDA UDI
Basic UDI-DI
B-08809260472150 EUDAMED
510(k) Number
K192561 FDA UDI
FDA Product Code
DZI FDA UDI
EMDN Code
L1899 ELECTROSURGERY INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Dental power tool system, line-powered FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.4120 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

Ultrasonic Surgical Series by Saeshin Precision Co., Ltd. — Class IIb — 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 807e2034-4614-44f5-8fee-71efdbc35e2e 61 fields · synced Jul 29, 2026
  • FDA UDI 8f3bf93e-eb42-44ea-a439-b5b0a4af7b90 34 fields · synced May 30, 2026