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Drypro Sd-Q2

FDA UDI

Class I (US FDA UDI)

by Konica Minolta, Inc.

Identity

Trade Name
DRYPRO SD-Q2 FDA UDI
Generic Name
Medical x-ray film, non-screen FDA UDI
Device Name
MEDICAL IMAGING FILM FDA UDI
Model / Reference
AE5X FDA UDI
Description
MEDICAL IMAGING FILM FDA UDI

Identifiers

Primary DI / UDI-DI
04560141950559 FDA UDI
FDA Product Code
IWZ FDA UDI
GMDN Term
Medical 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

Category: Medical x-ray film, non-screen

Drypro Sd-Q2 by Konica Minolta, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Konica Minolta, Inc.

Sources (1)

  • FDA UDI 37c7c311-b2f5-4814-a2aa-9c728994a43f 35 fields · synced May 30, 2026