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Vivid iq
EUDAMEDFDA UDIClass IIa (EU MDR)
Ref Vivid iq v206 to v208 SW only upgrade kit/5951460Model Vivid iq
Identity
- Trade Name
- Vivid FDA UDI
- Generic Name
- Cardiovascular ultrasound imaging system FDA UDI
- Device Name
- Vivid iq EUDAMEDVivid iq V206 to V208 SW only upgrade kit with package FDA UDI
- Model / Reference
- Vivid iq EUDAMEDVivid iq v206 to v208 SW only upgrade kit/5951460 EUDAMEDiq v206 to v208 SW only upgrade kit FDA UDI
- Description
- Vivid iq V206 to V208 SW only upgrade kit with package FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00195278797551 EUDAMEDFDA UDI
- Basic UDI-DI
- 8406821BUG00254HD EUDAMED
- Direct Marketing DI
- 00195278797551 EUDAMED
- 510(k) Number
- K243620 FDA UDI
- FDA Product Code
- IYN FDA UDIIYO FDA UDIITX FDA UDI
- EMDN Code
- Z11040102 CARDIOLOGY ULTRASOUND SCANNERS EUDAMED
- GMDN Term
- Cardiovascular ultrasound imaging system FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 892.1550 FDA UDI892.1560 FDA UDI892.1570 FDA UDI
- Market of Registration
- France 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
Yes
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
Yes
FDA UDI
MR Unsafe FDA UDI
Vivid iq by GE Medical Systems CO. Ltd — 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 | 8406821BUG00254HD | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- GE Medical Systems CO. Ltd
- EUDAMED SRN
- CN-MF-000001856
- Authorised Representative
- GE Medical Systems SCS FR-AR-000000344
Sources (2)
- EUDAMED a27f4677-23c8-434a-bc25-912421883e67 61 fields · synced Oct 6, 2026
- FDA UDI eb82a405-86ff-4479-803d-ad037ededa0a 34 fields · synced May 30, 2026