Identity
- Trade Name
- Aprikos EUDAMED
- Device Name
- LP-27 Probes EUDAMED
- Model / Reference
- AM07-124-02 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07073371024145 EUDAMED
- Basic UDI-DI
- 7073371FILENO27X9 EUDAMED
- Direct Marketing DI
- 07073371024145 EUDAMED
- EMDN Code
- L031101 FISTULA PROBES, REUSABLE EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Norway EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
Yes
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
Aprikos by Aprikos Medical AS — 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 | 7073371FILENO27X9 | Class I | Active |
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Manufacturer
- Manufacturer
- Aprikos Medical AS
- EUDAMED SRN
- NO-MF-000044411
Sources (1)
- EUDAMED e7948149-6108-4108-9ef6-58f809651b06 61 fields · synced Jun 20, 2026