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Surgical Pack

EUDAMED

Class I (EU MDR)

Ref /

by PureMED Product (Yangzhou) Co., Ltd.

Identity

Device Name
Surgical Pack EUDAMED
Model / Reference
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06974837949990 EUDAMED
Basic UDI-DI
69748379401C0035S EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) EUDAMED

Classification

Device Class
Class I 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

Surgical Pack by PureMED Product (Yangzhou) 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-000013490
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED 0e8b256d-d276-415d-a91f-58d600d037ee 61 fields · synced Jul 11, 2026