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Dentus M2 Comfort

FDA UDI

Class I (US FDA UDI)

by Agfa Corp.

Identity

Trade Name
Dentus M2 Comfort FDA UDI
Generic Name
Dental x-ray film, non-screen FDA UDI
Model / Reference
DENTUS M2 Comfort 2x3cm FDA UDI

Identifiers

Catalog Number
34HOS FDA UDI
Primary DI / UDI-DI
05414904038673 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
Dental x-ray film, non-screen FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1840 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
Length — 2 Centimeter FDA UDI
Width — 3 Centimeter FDA UDI

Category: Dental x-ray film, non-screen

Dentus M2 Comfort by Agfa Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental x-ray film, non-screen.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agfa Corp.

Sources (1)

  • FDA UDI 24e19c3f-da6b-46bc-923b-897fd807d421 36 fields · synced May 30, 2026