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All Purpose Gel Pack (x2)

EUDAMED

Class I (EU MDR)

Ref /Model AMHX10Model C502B0

by Wuhan Pakcare Bio‐technology Co., Ltd.

Identity

Trade Name
All Purpose Gel Pack (x2) EUDAMED
Device Name
All Purpose Gel Pack (x2) EUDAMED
Reusable Hot/cold packs EUDAMED
Model / Reference
AMHX10 EUDAMED
/ EUDAMED
C502B0 EUDAMED

Identifiers

Primary DI / UDI-DI
06973589091421 EUDAMED
Basic UDI-DI
B-06973589091421 EUDAMED
697358909HP100MD EUDAMED
Direct Marketing DI
06973589091421 EUDAMED
EMDN Code
M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

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

Category: Hot/cold therapy pack, reusable

All Purpose Gel Pack (x2) by Wuhan Pakcare Bio‐technology Co., Ltd. — Class I — MDR, MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Hot/cold therapy pack, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
CN-MF-000008960
Authorised Representative
Share info GmbH DE-AR-000005132

Sources (2)

  • EUDAMED c84a3055-65e7-4295-8433-b01b96f32009 61 fields · synced Jul 26, 2026
  • EUDAMED b29e1287-2b46-44de-9652-d75359b54285 61 fields · synced May 19, 2026