Identity
- Device Name
- IM-1060 TUBEGUARD EUDAMED
- Model / Reference
- IM-1060 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 05902596226565 EUDAMED
- Basic UDI-DI
- B-05902596226565 EUDAMED
- EMDN Code
- G030804,R01038099 EUDAMED
Classification
- Device Class
- Class I EUDAMED
- Market of Registration
- Poland EUDAMED
Clinical & Handling
Sterile
Yes
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
Yes
EUDAMED
Reprocessed
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Im-1060 Tubeguard by Inoris Medical Sp. Z O.o. — Class I — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-05902596226565 | Class I | Active |
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Manufacturer
- Manufacturer
- Inoris Medical Sp. Z O.o.
- EUDAMED SRN
- PL-MF-000016864
Sources (1)
- EUDAMED da4b081f-7939-41cb-a471-0a709384b733 61 fields · synced Oct 6, 2026