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Floor Stand

FDA UDI

Class II (US FDA UDI)

by Bracco Injeneering

Identity

Trade Name
Floor Stand FDA UDI
Generic Name
CT contrast medium injection system, line-powered, mobile FDA UDI
Model / Reference
640076 FDA UDI

Identifiers

Catalog Number
640076 FDA UDI
Primary DI / UDI-DI
17630039300149 FDA UDI
510(k) Number
K151048 FDA UDI
FDA Product Code
IZQ FDA UDI
GMDN Term
CT contrast medium injection system, line-powered, mobile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1650 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

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 951d2259-230a-47ec-b27a-4b1640bd148b 37 fields · synced Jun 8, 2026