← Back to catalogue

Clear Image Devices

FDA UDI

Class I (US FDA UDI)

by Clear Image Devices Llc

Identity

Trade Name
Clear Image Devices FDA UDI
Generic Name
X-ray film cassette holder FDA UDI
Device Name
Bucky Protector FDA UDI
Model / Reference
CD-1919 FDA UDI
Description
Bucky Protector FDA UDI

Identifiers

Catalog Number
1919 FDA UDI
Primary DI / UDI-DI
00811571030002 FDA UDI
FDA Product Code
IXY FDA UDI
GMDN Term
X-ray film cassette holder FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1880 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

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

Yes

FDA UDI

Category: X-ray film cassette holder

Clear Image Devices by Clear Image Devices Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as X-ray film cassette holder.

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

Sources (1)

  • FDA UDI dfd50e24-41de-4709-901a-56fd7e7cc010 34 fields · synced May 31, 2026