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Therasound Evo Package

FDA UDI

Class II (US FDA UDI)

by Compass Health Brands Corp.

Identity

Trade Name
THERASOUND EVO PACKAGE FDA UDI
Generic Name
Ultrasound coupling pad holder FDA UDI
Device Name
THERASOUND EVO 220, THERAPY HAMMER,AUTOSOUND, LEAD CORDS, 5CM GELSHOTS & ADAPTORS FDA UDI
Model / Reference
410-020-220 FDA UDI
Description
THERASOUND EVO 220, THERAPY HAMMER,AUTOSOUND, LEAD CORDS, 5CM GELSHOTS & ADAPTORS FDA UDI

Identifiers

Primary DI / UDI-DI
00852515007155 FDA UDI
FDA Product Code
MUI FDA UDI
IMI FDA UDI
GMDN Term
Ultrasound coupling pad holder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1570 FDA UDI
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

No

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

Therasound Evo Package 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 4fa75007-6e26-4ab2-983a-63f8faa34951 35 fields · synced Jun 8, 2026