← Back to catalogue

imagiQ

FDA UDI

Class I (US FDA UDI)

by Stille AB

Identity

Trade Name
imagiQ FDA UDI
Generic Name
Fluoroscopy/angiography table, powered FDA UDI
Device Name
Factory installed upgrade for imagiQ2 table, non visible, built into the final device. FDA UDI
Model / Reference
Performance kit FDA UDI
Description
Factory installed upgrade for imagiQ2 table, non visible, built into the final device. FDA UDI

Identifiers

Catalog Number
535-1712 FDA UDI
Primary DI / UDI-DI
07332339222130 FDA UDI
FDA Product Code
GDC FDA UDI
GMDN Term
Fluoroscopy/angiography table, powered FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

No

FDA UDI

Category: Fluoroscopy/angiography table, powered

imagiQ by Stille AB — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluoroscopy/angiography table, powered.

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
Stille AB

Sources (1)

  • FDA UDI 6fdf257d-7e92-4c88-b551-4213d7ea7ea4 35 fields · synced May 30, 2026