← Back to catalogue

DRYVIEW DVB Laser Imaging Film

FDA UDI

Class I (US FDA UDI)

by Carestream Health, Inc.

Identity

Trade Name
DRYVIEW DVB Laser Imaging Film FDA UDI
Generic Name
Medical x-ray film, non-screen FDA UDI
Device Name
125SH 25X30CM (10X12IN) DVB IN FDA UDI
Model / Reference
DRYVIEW DVB Laser Imaging Film FDA UDI
Description
125SH 25X30CM (10X12IN) DVB IN FDA UDI

Identifiers

Catalog Number
1752062 FDA UDI
Primary DI / UDI-DI
40889971752068 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Medical x-ray film, non-screen

DRYVIEW DVB Laser Imaging Film by Carestream Health, 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

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

Manufacturer

Manufacturer
Carestream Health, Inc.

Sources (1)

  • FDA UDI ca00caf1-144e-4ae3-bd92-b1cd81da1727 34 fields · synced Jun 8, 2026