Identity
- Trade Name
- Uriflet S 9HA EUDAMED
- Device Name
- Uriflet S 9HA EUDAMED
- Model / Reference
- 73521 EUDAMED
Identifiers
- Primary DI / UDI-DI
- D-73521HH EUDAMED
- Basic UDI-DI
- B-73521HH EUDAMED
- EMDN Code
- W0101060205 URINE MULTI-CONSTITUENT TEST STRIPS (AUTOMATED) EUDAMED
Classification
- Device Class
- Class IVD General EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Microbial Substances
Yes
EUDAMED
Reagent
Yes
EUDAMED
Self Testing
No
EUDAMED
Near-Patient Testing
No
EUDAMED
Professional Testing
Yes
EUDAMED
Companion Diagnostics
No
EUDAMED
Surgical Instrument
No
EUDAMED
Uriflet S 9HA by ARKRAY Factory, Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/IVDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/IVDD | B-73521HH | Class IVD General | Active |
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Manufacturer
- Manufacturer
- ARKRAY Factory, Inc.
- EUDAMED SRN
- JP-MF-000003008
- Authorised Representative
- ARKRAY Europe, B.V. NL-AR-000002056
Sources (1)
- EUDAMED 67976ac2-69bb-459e-85a7-e4d121d44bf8 61 fields · synced Jul 24, 2026