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Amtouch

FDA UDI

Class I (US FDA UDI)

by American Medical & Hospital Supply Co., Inc.

Identity

Trade Name
Amtouch FDA UDI
Generic Name
Medical device cleaning agent FDA UDI
Device Name
Ultrasonic Cleaning Solution, Liquid, Tartar & Stain Remover - 128 fl oz - 1/bottle FDA UDI
Model / Reference
Ultrasonic Cleaner - Tartar & Stain FDA UDI
Description
Ultrasonic Cleaning Solution, Liquid, Tartar & Stain Remover - 128 fl oz - 1/bottle FDA UDI

Identifiers

Catalog Number
AM-UCTS FDA UDI
Primary DI / UDI-DI
00850058951195 FDA UDI
FDA Product Code
FLG FDA UDI
GMDN Term
Medical device cleaning agent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6150 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Total Volume — 128 Fluid Ounce FDA UDI
Total Volume — 3.78 Liter FDA UDI

Category: Medical device cleaning agent

Amtouch by American Medical & Hospital Supply Co., Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Medical device cleaning agent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0b3ccd89-2a41-4b8d-8b5a-66a373745dbc 35 fields · synced Jun 8, 2026