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Therasound3 Standard 120V

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
Therasound3 Standard 120V FDA UDI
Generic Name
Physical therapy ultrasound system FDA UDI
Device Name
Therasound 3 Standard Device Only (120V) FDA UDI
Model / Reference
410-026 FDA UDI
Description
Therasound 3 Standard Device Only (120V) FDA UDI

Identifiers

Primary DI / UDI-DI
00092237901236 FDA UDI
FDA Product Code
IMI FDA UDI
GMDN Term
Physical therapy ultrasound system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5300 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

Therasound3 Standard 120V by Compass Health Brands Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 13fa28a3-347c-4124-ab69-471762bf7c55 35 fields · synced Jun 8, 2026