← Back to catalogue
Saliva Ejector
EUDAMEDClass I (EU MDR)
Ref AT008Model AT008, AT009 ,AT010,AT011
Identity
- Device Name
- Saliva Ejector EUDAMED
- Model / Reference
- AT008, AT009 ,AT010,AT011 EUDAMEDAT008 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06975336240441 EUDAMED
- Basic UDI-DI
- 697533624SE001GF EUDAMED
- EMDN Code
- Q019001 SALIVA ASPIRATORS AND SALIVA ABSORBENTS EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Austria 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
Saliva Ejector by Rocodent International Limited — 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 | 697533624SE001GF | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Rocodent International Limited
- EUDAMED SRN
- CN-MF-000045441
- Authorised Representative
- SUNGO Europe B.V. NL-AR-000000247
Sources (1)
- EUDAMED c4f9b6dd-4248-4ff6-b5a2-c08fc12c8f81 61 fields · synced Jun 18, 2026