← Back to catalogue

Injector

FDA UDI

Class II (US FDA UDI)

by Bracco Injeneering

Identity

Trade Name
Injector FDA UDI
Generic Name
CT contrast medium injection system, line-powered, stationary FDA UDI
Model / Reference
102410 FDA UDI

Identifiers

Catalog Number
102410 FDA UDI
Primary DI / UDI-DI
17630039301450 FDA UDI
FDA Product Code
JAK FDA UDI
IZQ FDA UDI
GMDN Term
CT contrast medium injection system, line-powered, stationary FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 FDA UDI
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: CT contrast medium injection system, line-powered, stationaryCT contrast medium injection system, line-powered, mobile

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

Similar devices

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

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
Bracco Injeneering

Sources (1)

  • FDA UDI cf7799dc-f076-4d7a-a141-ddbfa7c79c29 34 fields · synced Jun 1, 2026