← Back to catalogue

iQ Elevation

FDA UDI

Class I (US FDA UDI)

by First Source Inc.

Identity

Trade Name
iQ Elevation FDA UDI
Generic Name
Radiological general body-part positioner FDA UDI
Device Name
A weight bearing stand that will allow a patient to be positioned for various U-Arm x-ray examinations of lower extremities. FDA UDI
Model / Reference
1 FDA UDI
Description
A weight bearing stand that will allow a patient to be positioned for various U-Arm x-ray examinations of lower extremities. FDA UDI

Identifiers

Catalog Number
100DRWBS FDA UDI
Primary DI / UDI-DI
G221100DRWBS0 FDA UDI
FDA Product Code
KXH FDA UDI
GMDN Term
Radiological general body-part positioner FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
892.1830 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: Radiological general body-part positioner

iQ Elevation by First Source Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiological general body-part positioner.

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
First Source Inc.

Sources (1)

  • FDA UDI d771b72a-2e9a-46b9-8abc-46ad6828497f 34 fields · synced May 30, 2026