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Pack Ivt N°3

EUDAMED

Class I (EU MDR)

Ref K1050

by Jiangsu Medplus Non-woven Manufacturer Co., Ltd.

Identity

Trade Name
PACK IVT N°3 EUDAMED
Device Name
Surgical Packs EUDAMED
Model / Reference
K1050 EUDAMED

Identifiers

Primary DI / UDI-DI
06971705248834 EUDAMED
Basic UDI-DI
697170524DLYS EUDAMED
EMDN Code
T0202 SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS) EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Pack Ivt N°3 by Jiangsu Medplus Non-woven Manufacturer 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-000022548
Authorised Representative
MedPath GmbH DE-AR-000000087

Sources (1)

  • EUDAMED 163da705-b469-4bdf-b744-dd7137b1b57b 61 fields · synced Jun 18, 2026