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Multi-frequency Convex-array Ultrasound Probe
EUDAMEDClass IIa (EU MDR)
Ref C5I20GModel C3L60K, C3L60A, C3L60C, C3L60G, C3L40C, C3L40G, C6LN, C6LC, C5L40K, C6L15K, C3I40, C3I60F, C3I60, C3I40F, C3L40A, C5I20, C5I40, C5I20G
Identity
- Device Name
- Multi-frequency Convex-array Ultrasound Probe EUDAMED
- Model / Reference
- C3L60K, C3L60A, C3L60C, C3L60G, C3L40C, C3L40G, C6LN, C6LC, C5L40K, C6L15K, C3I40, C3I60F, C3I60, C3I40F, C3L40A, C5I20, C5I40, C5I20G EUDAMEDC5I20G EUDAMED
Identifiers
- Primary DI / UDI-DI
- 06938396492052 EUDAMED
- Basic UDI-DI
- 693839640010042771K00005K EUDAMED
- EMDN Code
- Z11040299 ULTRASOUND PROBES – OTHER EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany 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
Multi-frequency Convex-array Ultrasound Probe by Shantou Institute of Ultrasonic Instruments Co., Ltd. — Class IIa — MDR — listed in EUDAMED
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 | 693839640010042771K00005K | Class IIa | Active |
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Manufacturer
- EUDAMED SRN
- CN-MF-000010834
- Authorised Representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Sources (1)
- EUDAMED abc6e005-3e21-4048-af62-5eccf4aef562 61 fields · synced Oct 8, 2026