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Mamoray Hd

FDA UDI

Class II (US FDA UDI)

by Agfa Corp.

Identity

Trade Name
MAMORAY HD FDA UDI
Generic Name
X-ray film cassette, manual FDA UDI
Device Name
MAMORAY CASSETTE / HD FDA UDI
Model / Reference
MAMORAY HD 24X30 FDA UDI
Description
MAMORAY CASSETTE / HD FDA UDI

Identifiers

Catalog Number
EDBVA FDA UDI
Primary DI / UDI-DI
05414904009802 FDA UDI
510(k) Number
K790273 FDA UDI
FDA Product Code
IZH FDA UDI
GMDN Term
X-ray film cassette, manual FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1710 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

Yes

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Width — 30 Centimeter FDA UDI
Length — 24 Centimeter FDA UDI

Category: X-ray film cassette, manual

Mamoray Hd by Agfa Corp. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette, manual.

Cleared under the same submission

K790273 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Agfa Corp.

Sources (1)

  • FDA UDI 2551ceed-fe23-4288-8686-c344a65aa228 37 fields · synced Jun 8, 2026