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Image Diagnostics, Inc

FDA UDI

Class I (US FDA UDI)

by Image Diagnostics, Inc.

Identity

Trade Name
IMAGE DIAGNOSTICS, INC FDA UDI
Generic Name
Radiation shielding curtain FDA UDI
Device Name
IDI,RADIATION SHIELD SYSTEM,PROTEGO,PROLITE TABLE MOUNT,METRIC ACCESSORY RAILS,PHILIPS TABLE#A800-0471-PH FDA UDI
Model / Reference
Protego ProLite System for Philips Tables FDA UDI
Description
IDI,RADIATION SHIELD SYSTEM,PROTEGO,PROLITE TABLE MOUNT,METRIC ACCESSORY RAILS,PHILIPS TABLE#A800-0471-PH FDA UDI

Identifiers

Catalog Number
A800-0471-PH FDA UDI
Primary DI / UDI-DI
00850061871176 FDA UDI
FDA Product Code
IWQ FDA UDI
GMDN Term
Radiation shielding curtain FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.6500 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Radiation shielding curtain

Image Diagnostics, Inc by Image Diagnostics, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation shielding curtain.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 230f6f0b-0939-4f53-b144-d1d24b668a08 35 fields · synced May 30, 2026