← Back to catalogue

Ez

FDA UDI

Class I (US FDA UDI)

by Centrix, Inc.

Identity

Trade Name
EZ FDA UDI
Generic Name
Dental material cartridge-plunging applicator, single-component FDA UDI
Device Name
EZ GUN WHITE FDA UDI
Model / Reference
130700 FDA UDI
Description
EZ GUN WHITE FDA UDI

Identifiers

Primary DI / UDI-DI
00817051023724 FDA UDI
FDA Product Code
EID FDA UDI
GMDN Term
Dental material cartridge-plunging applicator, single-component FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Ez by Centrix, Inc. — 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Centrix, Inc.

Sources (1)

  • FDA UDI 58d01e43-33dd-4df7-b89e-61daa11310bf 33 fields · synced May 30, 2026