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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
TABLE, OPERATINGROOM, ELECTRICAL FDA UDI
Model / Reference
imagiQ2 FDA UDI
Description
TABLE, OPERATINGROOM, ELECTRICAL FDA UDI

Identifiers

Catalog Number
530-1703 FDA UDI
Primary DI / UDI-DI
07332339222062 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

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

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Manufacturer

Manufacturer
Stille AB

Sources (1)

  • FDA UDI de0afaae-3d69-4b99-bf0b-7d8128bef99d 35 fields · synced May 30, 2026