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Empower MR Injector Head

FDA UDI

Class II (US FDA UDI)

by Bracco Injeneering

Identity

Trade Name
Empower MR Injector Head FDA UDI
Generic Name
MRI contrast medium injection system, line-powered, mobile FDA UDI
Model / Reference
017377 FDA UDI

Identifiers

Catalog Number
017377 FDA UDI
Primary DI / UDI-DI
17630039301016 FDA UDI
510(k) Number
K062449 FDA UDI
FDA Product Code
IZQ FDA UDI
GMDN Term
MRI contrast medium injection system, line-powered, mobile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 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

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: MRI contrast medium injection system, line-powered, mobile

Empower MR Injector Head by Bracco Injeneering — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as MRI contrast medium injection system, line-powered, mobile.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bracco Injeneering

Sources (1)

  • FDA UDI 307575e8-813b-4e80-afea-00a54f886218 35 fields · synced Jun 1, 2026