← Back to catalogue
T Lite Pro
EUDAMEDFDA UDIFDA 510(k)Class IIa (EU MDR)
Ref T LITE PROModel HANDHELD ULTRASOUND SCANNERS
by Sonoscanner
Identity
- Trade Name
- T LITE PRO EUDAMEDT Lite FDA UDI
- Generic Name
- General-purpose ultrasound imaging system FDA UDI
- Device Name
- Handheld Ultrasound Scanner T Lite Pro with exchangeables probes FDA UDI
- Model / Reference
- HANDHELD ULTRASOUND SCANNERS EUDAMEDT LITE PRO EUDAMEDPRO FDA UDI
- Description
- Handheld Ultrasound Scanner T Lite Pro with exchangeables probes FDA UDI
Identifiers
- Primary DI / UDI-DI
- 03701104600321 EUDAMEDFDA UDI
- Basic UDI-DI
- 37011046USHANDHELDTS EUDAMED
- Direct Marketing DI
- 03701104600321 EUDAMED
- 510(k) Number
- K232285 FDA UDI
- FDA Product Code
- IYO FDA UDIIYN FDA UDI
- EMDN Code
- Z11040106 HANDHELD 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 UDI892.1550 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
T Lite Pro by Sonoscanner — Class IIa — FDA_510K, MDR — listed in EUDAMED, FDA GUDID, FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
United States Active
FDA_510K
European Union Active
CE/MDR
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K201988 | Class IIa | Active |
| EUDAMED | European Union | CE/MDR | 37011046USHANDHELDTS | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Sonoscanner
- EUDAMED SRN
- FR-MF-000002220
Sources (3)
- EUDAMED 872d0fe6-1a9b-4735-8e05-aa1f26565111 61 fields · synced Oct 6, 2026
- FDA UDI 5d288e76-9722-4f42-a3e0-640dbfc87b09 34 fields · synced May 30, 2026
- FDA 510(k) K201988 1 fields · synced May 18, 2026