Identity
- Trade Name
- Ultrasonix Medical Corporation FDA UDI
- Generic Name
- General-purpose ultrasound imaging system FDA UDI
- Device Name
- SonixSP Q+Ultrasound System FDA UDI
- Model / Reference
- 22.000.000-02 FDA UDI
- Description
- SonixSP Q+Ultrasound System FDA UDI
Identifiers
- Primary DI / UDI-DI
- 08294362200020 FDA UDI
- FDA Product Code
- IYN 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 UDI892.1560 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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Ultrasonix Medical Corporation by Analogic Corporation — 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
- Analogic Corporation
Sources (1)
- FDA UDI 90240871-bdd1-491d-9017-7b0f4ec53709 35 fields · synced May 31, 2026