Ultrasite® 473446

by B. Braun Medical, Inc.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number04046964185328 UDI-DI	Date5 Jan 2017Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: Ultrasite®
Generic Name: Intravenous administration tubing extension set
Model / Ref / Catalog: 473446
Description: CSE6SB ULTRASITE EXT SET 8 IN.

Primary DI / UDI-DI: 04046964185328
FDA Product Code: FPA
GMDN Term: Intravenous administration tubing extension set

Device Class: Class II
Regulation Number: 880.5440
GUDID distribution status: In Commercial Distribution

Other devices from B. Braun Medical, Inc.

See all devices from B. Braun Medical, Inc. →

Properties

Sterile
Single Use
Prescription Use
Lot / Batch Number
Expiration Date

Other properties (9)

Implantable: No
Contains Latex: No
Over-the-Counter: No
Convenience Kit: No
Combination Product: No
HCT/P: No
Premarket Exempt: No
Serial Number: No
Manufacturing Date: No