Identity
- Trade Name
- KaVo DRYspray™ EUDAMED
- Device Name
- KaVo DRYspray™ EUDAMED
- Model / Reference
- 10070580 EUDAMED
Identifiers
- Primary DI / UDI-DI
- +E251100705801 EUDAMED
- Basic UDI-DI
- ++E251200038018W EUDAMED
- Direct Marketing DI
- +E251100705801 EUDAMED
- EMDN Code
- V80 CLINICAL USE ACCESSORIES NOT INCLUDED IN OTHER CLASSES 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
KaVo DRYspray™ by Alpro Medical Gmbh — 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 | ++E251200038018W | Class I | Active |
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Manufacturer
- Manufacturer
- Alpro Medical Gmbh
- EUDAMED SRN
- DE-MF-000010603
Sources (1)
- EUDAMED b646cb2d-0343-4358-9cb7-baec93b6704e 61 fields · synced Jun 18, 2026