Identity
- Trade Name
- Vscan FDA UDI
- Generic Name
- General-purpose ultrasound imaging system FDA UDI
- Device Name
- Vscan Gateway SW - V1.4.2 FDA UDI
- Model / Reference
- Gateway v.1.4 FDA UDI
- Description
- Vscan Gateway SW - V1.4.2 FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00840682115384 FDA UDI
- FDA Product Code
- IYN FDA UDIITX FDA UDIIYO FDA UDI
- GMDN Term
- General-purpose ultrasound imaging system FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 892.1550 FDA UDI892.1570 FDA UDI892.1560 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Vscan by Ge Vingmed Ultrasound — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Ge Vingmed Ultrasound
Sources (1)
- FDA UDI ecafa200-c80d-44ab-81b6-d65715577db2 35 fields · synced Jun 6, 2026