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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
Arm procedure positioner, reusable FDA UDI
Device Name
IDI,VASCULAR ARM BOARD,LOW-PROFILE,#A100-2244 FDA UDI
Model / Reference
LOW-PROFILE VAB FDA UDI
Description
IDI,VASCULAR ARM BOARD,LOW-PROFILE,#A100-2244 FDA UDI

Identifiers

Catalog Number
A100-2244 FDA UDI
Primary DI / UDI-DI
00850977007607 FDA UDI
FDA Product Code
NOD FDA UDI
GMDN Term
Arm procedure positioner, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.3910 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: Arm procedure positioner, reusable

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

Similar devices

Also classified as Arm procedure positioner, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 0cca1b87-05ca-4a09-ac1b-5e57a4c5e187 35 fields · synced May 30, 2026