Identity
- Trade Name
- Freka® Universal Funnel Adaptor, ENFit EUDAMED
- Device Name
- enteral class I EUDAMED
- Model / Reference
- 7755695 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04250273725483 EUDAMED
- Basic UDI-DI
- 42502737NEN60011x000000RZ EUDAMED
- Unit of Use DI
- 04250273759389 EUDAMED
- EMDN Code
- A0380 TUBULAR DEVICES - ACCESSORIES 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
Freka® Universal Funnel Adaptor, ENFit by Fresenius Kabi AG — Class I — 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 | 42502737NEN60011x000000RZ | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fresenius Kabi AG
- EUDAMED SRN
- DE-MF-000009273
Sources (1)
- EUDAMED a6eaef65-c26b-4ef1-819a-b7f5d3318c17 61 fields · synced Jul 24, 2026