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Super-Bond C&B Red Activator

EUDAMED

Class IIa (EU MDR)

Ref T030ERef T030T

by Sun Medical Co., Ltd.

Identity

Trade Name
Super-Bond C&B Red Activator EUDAMED
Device Name
Super-Bond EUDAMED
Model / Reference
T030E EUDAMED
T030T EUDAMED

Identifiers

Primary DI / UDI-DI
04560227801720 EUDAMED
04560227801737 EUDAMED
Basic UDI-DI
B-04560227801720 EUDAMED
B-04560227801737 EUDAMED
EMDN Code
Q0101010299,Q010407 EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
France EUDAMED
Türkiye EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

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

Super-Bond C&B Red Activator by Sun Medical Co., Ltd. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
JP-MF-000011109
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED cc49e7ff-4af7-4e76-8262-daa664e9620c 61 fields · synced Jul 29, 2026
  • EUDAMED 7f115056-d954-46cf-b662-e8208b258de2 61 fields · synced May 17, 2026