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Terason

FDA UDI

Class II (US FDA UDI)

by Teratech Corporation

Identity

Trade Name
Terason FDA UDI
Generic Name
Hand-held ultrasound imaging system, body-surface FDA UDI
Device Name
The Terason uSmart3200T Cart is used to provide a portable solution-On-Wheels for the Terason uSmart3200T Ultrasound Imaging System. FDA UDI
Model / Reference
uSmart3200T FDA UDI
Description
The Terason uSmart3200T Cart is used to provide a portable solution-On-Wheels for the Terason uSmart3200T Ultrasound Imaging System. FDA UDI

Identifiers

Primary DI / UDI-DI
00852698007416 FDA UDI
FDA Product Code
IYN FDA UDI
IYO FDA UDI
ITX FDA UDI
GMDN Term
Hand-held ultrasound imaging system, body-surface FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1550 FDA UDI
892.1560 FDA UDI
892.1570 FDA UDI
Commercial Distribution
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

No

FDA UDI

Category: Hand-held ultrasound imaging system, body-surface

Terason by Teratech Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hand-held ultrasound imaging system, body-surface.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5b3ff4ae-2695-4c69-aecb-e2c58c9f992f 34 fields · synced Jun 7, 2026