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Compresse lin universelle kinedolin
EUDAMEDClass I (EU MDR)
Ref 700Model kinedolin
Identity
- Trade Name
- Compresse lin universelle kinedolin EUDAMED
- Device Name
- Compresse lin universelle kinedolin EUDAMED
- Model / Reference
- kinedolin EUDAMED700 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06192313400012 EUDAMED
- Basic UDI-DI
- 6192313400018T EUDAMED
- Direct Marketing DI
- 06192313400012 EUDAMED
- EMDN Code
- M9001 CRYOTHERAPY AND THERMOTHERAPY DEVICES EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- France 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
Compresse lin universelle kinedolin by Kine L'ayptis Labo — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS
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Also classified as Hot/cold therapy pack, reusable.
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- reusable cold hot gel pack for Ankle — Wuhan Pakcare Bio‐technology Co.,Ltd. · Class I
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 6192313400018T | Class I | Active |
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Manufacturer
- Manufacturer
- Kine L'ayptis Labo
- EUDAMED SRN
- TN-MF-000020714
- Authorised Representative
- kipocora FR-AR-000017148
Sources (1)
- EUDAMED d587cb1e-6c11-46ef-8e26-2b8e2487cab6 61 fields · synced Aug 4, 2026