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InnoSight
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref 9J.3AHUS.P05Model InnoSight/T3300/H1300
Identity
- Trade Name
- InnoSight EUDAMEDInnoSight Diagnostic Ultrasound System FDA UDI
- Generic Name
- General-purpose ultrasound imaging system FDA UDI
- Device Name
- Diagnostic Ultrasound System EUDAMEDInnoSight Diagnostic Ultrasound System FDA UDI
- Model / Reference
- InnoSight/T3300/H1300 EUDAMED9J.3AHUS.P05 EUDAMED989605486132 FDA UDI
- Description
- InnoSight Diagnostic Ultrasound System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 04719873000517 EUDAMEDFDA UDI
- Basic UDI-DI
- 471987300VIVAPRO5J EUDAMED
- Direct Marketing DI
- 04719873000517 EUDAMED
- FDA Product Code
- IYO FDA UDIITX FDA UDIIYN FDA UDI
- EMDN Code
- Z11040103 PORTABLE ULTRASOUND SCANNERS EUDAMED
- GMDN Term
- General-purpose ultrasound imaging system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1560 FDA UDI892.1570 FDA UDI892.1550 FDA UDI
- Market of Registration
- Ireland EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
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
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
InnoSight by Qisda Corporation — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 471987300VIVAPRO5J | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Qisda Corporation
- EUDAMED SRN
- TW-MF-000010709
- Authorised Representative
- MedNet EC-REP GmbH DE-AR-000000002
Sources (2)
- EUDAMED 29cf20de-76e9-4ad0-9e58-ffb33f33bd40 61 fields · synced May 29, 2026
- FDA UDI 7fb8cf6c-2860-44c0-9487-7f33d5ac8480 33 fields · synced May 27, 2026