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American Medicals

FDA UDI

Class I (US FDA UDI)

by American Medicals

Identity

Trade Name
American Medicals FDA UDI
Generic Name
Dental material cartridge-plunging applicator, single-component FDA UDI
Model / Reference
1 FDA UDI

Identifiers

Primary DI / UDI-DI
B35682602180 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Dental material cartridge-plunging applicator, single-component FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Microwave Radiation FDA UDI

Category: Dental material cartridge-plunging applicator, single-component

American Medicals by American Medicals — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental material cartridge-plunging applicator, single-component.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
American Medicals

Sources (1)

  • FDA UDI 90e07178-47fd-4904-b1d3-ff9ff6125e3e 32 fields · synced Jun 8, 2026