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Robotic Ultrasound System (Patient-end) MGIUS-R3P EXP
EUDAMEDClass IIa (EU MDR)
Ref 900-000220-00
Identity
- Trade Name
- Robotic Ultrasound System (Patient-end) MGIUS-R3P EXP EUDAMED
- Device Name
- Robotic Ultrasound System EUDAMED
- Model / Reference
- 900-000220-00 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06974318130756 EUDAMED
- Basic UDI-DI
- B-06974318130756 EUDAMED
- EMDN Code
- Z11040199 ULTRASOUND SCANNERS - OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Latvia EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
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
Robotic Ultrasound System (Patient-end) MGIUS-R3P EXP by Wuhan MGI Tech Co., Ltd. — Class IIa — 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-06974318130756 | Class IIa | Active |
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Manufacturer
- Manufacturer
- Wuhan MGI Tech Co., Ltd.
- EUDAMED SRN
- CN-MF-000018732
- Authorised Representative
- Latvia MGI Tech SIA LV-AR-000017789
Sources (1)
- EUDAMED bc88259a-3305-433c-8411-630a56517df0 61 fields · synced Oct 6, 2026