← Back to catalogue

Transfer Set

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name
Transfer Set FDA UDI
Generic Name
Fluid transfer set, general-purpose FDA UDI
Device Name
Fluid Transfer Set (V1905) FDA UDI
Model / Reference
V1905 FDA UDI
Description
Fluid Transfer Set (V1905) FDA UDI

Identifiers

Catalog Number
V1905 FDA UDI
Primary DI / UDI-DI
04046964188534 FDA UDI
FDA Product Code
FPA FDA UDI
GMDN Term
Fluid transfer set, general-purpose 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fluid transfer set, general-purpose

Transfer Set by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fluid transfer set, general-purpose.

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

Sources (1)

  • FDA UDI ccc12fa3-1b40-400f-b66e-04fc7315ed86 35 fields · synced Jun 1, 2026