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Universal pack

EUDAMED

Class I (EU MDR)

Ref 520939Model General Surgical Pack

by Cobes Industries(Hefei) Co., Ltd

Identity

Trade Name
Universal pack EUDAMED
Device Name
General Surgical Pack EUDAMED
Model / Reference
General Surgical Pack EUDAMED
520939 EUDAMED

Identifiers

Primary DI / UDI-DI
06956288660631 EUDAMED
Basic UDI-DI
69562886MA0004LG EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Universal pack by Cobes Industries(Hefei) Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000012364
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 517136e0-abe6-4891-a7e4-3dff28d5ed96 61 fields · synced Jun 19, 2026