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Liflow® 3.0
EUDAMEDClass IIa (EU MDR)
Ref Liflow® 3.0Model Liflow
by Intrasense
Identity
- Trade Name
- Liflow® 3.0 EUDAMED
- Device Name
- Liflow EUDAMED
- Model / Reference
- Liflow EUDAMEDLiflow® 3.0 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 03700719701096 EUDAMED
- Basic UDI-DI
- 37007197LiflowAQ EUDAMED
- Direct Marketing DI
- 03700719701096 EUDAMED
- EMDN Code
- Z11069082 VARIOUS DIGITAL BIOIMAGING MANAGEMENT INSTRUMENTS - SOFTWARE ACCESSORIES EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Special Device Type
- Software 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
Yes
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Liflow® 3.0 by Intrasense — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS
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 | 37007197LiflowAQ | Class IIa | Active |
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Manufacturer
- Manufacturer
- Intrasense
- EUDAMED SRN
- FR-MF-000001551
Sources (1)
- EUDAMED 23b28d07-aa85-49fe-88c9-cb2353b33b0d 61 fields · synced Jun 17, 2026