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SOS BOBO DINO pack

EUDAMED

Class I (EU MDR)

Ref AMFX03Model C502B0Ref /

by Wuhan Pakcare Bio‐technology Co., Ltd.

Identity

Trade Name
SOS BOBO DINO pack EUDAMED
Device Name
Reusable Hot/cold packs EUDAMED
SOS BOBO DINO pack EUDAMED
Model / Reference
C502B0 EUDAMED
AMFX03 EUDAMED
/ EUDAMED

Identifiers

Primary DI / UDI-DI
06973589091131 EUDAMED
Basic UDI-DI
697358909HP100MD EUDAMED
B-06973589091131 EUDAMED
Direct Marketing DI
06973589091131 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

SOS BOBO DINO pack by Wuhan Pakcare Bio‐technology Co., Ltd. — Class I — MDD, MDR — 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/MDD

European Union Active

CE/MDR

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Manufacturer

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

Sources (2)

  • EUDAMED 20f51048-6ea2-4bd5-a952-4691a29fe016 61 fields · synced Jun 18, 2026
  • EUDAMED 4caaef4c-c445-46d9-bb0e-848b8bec54cb 61 fields · synced May 19, 2026