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Magnus

FDA UDI

Class II (US FDA UDI)

by Maquet, Inc.

Identity

Trade Name
MAGNUS FDA UDI
Generic Name
Angiographic x-ray system table, powered FDA UDI
Device Name
MAGNUS carbon-fibre table top FDA UDI
Model / Reference
1180.16F2 FDA UDI
Description
MAGNUS carbon-fibre table top FDA UDI

Identifiers

Catalog Number
1180.16F2 FDA UDI
Primary DI / UDI-DI
04046768040809 FDA UDI
FDA Product Code
KXJ FDA UDI
GMDN Term
Angiographic x-ray system table, powered FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1980 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: Angiographic x-ray system table, powered

Magnus by Maquet, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Angiographic x-ray system table, powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Maquet, Inc.

Sources (1)

  • FDA UDI 824a8081-612f-461a-885f-9664311aa0d2 34 fields · synced May 30, 2026