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Amtouch Temporary Crown & Bridge Material

FDA UDI

Class II (US FDA UDI)

by American Medical & Hospital Supply Co., Inc.

Identity

Trade Name
Amtouch Temporary Crown & Bridge Material FDA UDI
Generic Name
Dental composite resin FDA UDI
Device Name
Amtouch Temporary Crown & Bridge Material - A2 (1x Cartridge, 10x Mixing Tips) FDA UDI
Model / Reference
A2 FDA UDI
Description
Amtouch Temporary Crown & Bridge Material - A2 (1x Cartridge, 10x Mixing Tips) FDA UDI

Identifiers

Catalog Number
AMTCBA2 FDA UDI
Primary DI / UDI-DI
00850048528925 FDA UDI
FDA Product Code
EBG FDA UDI
GMDN Term
Dental composite resin FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3770 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Dental composite resin

Amtouch Temporary Crown & Bridge Material by American Medical & Hospital Supply Co., Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Dental composite resin.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 08b2f721-9bb5-41ab-a8dc-547a27fc0d95 35 fields · synced May 30, 2026