Identity
- Device Name
- Kilroid EUDAMEDKilRoid, Haemorrhoid suction ligator EUDAMED
- Model / Reference
- 67401 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 07395502089558 EUDAMED
- Basic UDI-DI
- 07395502061241479E EUDAMED
- Direct Marketing DI
- 07395502089558 EUDAMED
- EMDN Code
- G020401 HAEMORRHOID LIGATURE SETS EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Sweden 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
Kilroid by Mediplast AB — 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 | 07395502061241479E | Class IIa | Active |
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Manufacturer
- Manufacturer
- Mediplast AB
- EUDAMED SRN
- SE-MF-000000885
Sources (2)
- EUDAMED 628b0140-9795-430a-83ee-677b3d08986a 61 fields · synced Jun 19, 2026
- EUDAMED a1f20a63-5138-485b-bb8a-906c90e1fdd5 61 fields · synced Jun 19, 2026