← Back to catalogue
Rusch Silkospray Universal Silicone Spray
EUDAMEDClass IIa (EU MDR)
Ref 556000-000000
Identity
- Trade Name
- Rusch Silkospray Universal Silicone Spray EUDAMED
- Device Name
- RÜSCH® Silkospray®, Universal Silicone Spray EUDAMED
- Model / Reference
- 556000-000000 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 10801902221596 EUDAMED
- Basic UDI-DI
- 08019020000000000000286L6 EUDAMED
- EMDN Code
- M9002 PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS) EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Ireland 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
Rusch Silkospray Universal Silicone Spray by Teleflex Medical — Class IIa — 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 | 08019020000000000000286L6 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Teleflex Medical
- EUDAMED SRN
- IE-MF-000015868
Sources (1)
- EUDAMED 1e956b29-fc42-495e-951d-f720ad8a1fd1 61 fields · synced Aug 2, 2026