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Polysonic

FDA UDI

Class II (US FDA UDI)

by Parker Laboratories, Inc.

Identity

Trade Name
POLYSONIC FDA UDI
Generic Name
Electrode conductive medium FDA UDI
Device Name
Polysonic Ultrasound Lotion, one gallon bottle FDA UDI
Model / Reference
ULTRASOUND LOTION FDA UDI
Description
Polysonic Ultrasound Lotion, one gallon bottle FDA UDI

Identifiers

Catalog Number
21-28 FDA UDI
Primary DI / UDI-DI
00855683006319 FDA UDI
FDA Product Code
IYO FDA UDI
GMDN Term
Electrode conductive medium FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electrode conductive medium

A comprehensive review of the Polysonic Ultrasound Lotion, including its features, compliance, and FAQs.

Similar devices

Also classified as Electrode conductive medium.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cc5ccd00-ad11-4df6-afc5-febc86855d3e 35 fields · synced Jul 24, 2026