Identity
- Trade Name
- Reliject Pre-Injection Swabs EUDAMED
- Device Name
- Pre-injection Swab EUDAMED
- Model / Reference
- 742 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05060131887425 EUDAMED
- Basic UDI-DI
- 506013188TF093U EUDAMED
- EMDN Code
- K01020109 MINIMALLY INVASIVE SURGERY SWABS EUDAMED
Classification
- Device Class
- Class I 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
Reliject Pre-Injection Swabs by Reliance Medical Ltd — 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 | 506013188TF093U | Class I | Active |
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Manufacturer
- Manufacturer
- Reliance Medical Ltd
- EUDAMED SRN
- GB-MF-000004799
- Authorised Representative
- Reliance Medical (Ireland) IE-AR-000003675
Sources (1)
- EUDAMED 14936270-0600-4609-9eb8-4bde87a26df7 61 fields · synced Jul 16, 2026