Solution Transfer Device

FDA UDI

Class II (US FDA UDI)

by Bracco Diagnostics Inc.

Identity

Trade Name: Solution Transfer Device FDA UDI
Generic Name: Radiographic procedure tubing FDA UDI
Device Name: US005110 I V Solution Transfer Kit FDA UDI
Model / Reference: 005110 FDA UDI
Description: US005110 I V Solution Transfer Kit FDA UDI

Identifiers

Catalog Number: 005110 FDA UDI
Primary DI / UDI-DI: 10815112020115 FDA UDI
FDA Product Code: FPA FDA UDI
GMDN Term: Radiographic procedure tubing FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Radiographic procedure tubing

Solution Transfer Device by Bracco Diagnostics Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Bracco Diagnostics Inc.

Sources (1)

FDA UDI 20bfeb1d-7221-4a1c-8d75-a27a9871b285 35 fields · synced Jun 8, 2026