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Philips Scanner Cable

FDA UDI

Class II (US FDA UDI)

by Bracco Injeneering

Identity

Trade Name
Philips Scanner Cable FDA UDI
Generic Name
CT contrast medium injection system, line-powered, stationary FDA UDI
Model / Reference
017613 FDA UDI

Identifiers

Catalog Number
017613 FDA UDI
Primary DI / UDI-DI
37630039300532 FDA UDI
FDA Product Code
DSB FDA UDI
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
870.2770 FDA UDI
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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: CT contrast medium injection system, line-powered, stationary

Philips Scanner Cable 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, stationary.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Bracco Injeneering

Sources (1)

  • FDA UDI debaed62-1108-4ef8-94d2-a66e3b55e6eb 35 fields · synced Jun 1, 2026