SafeDAY™ 352646

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	Number04046955626946 UDI-DI	Date21 Jul 2020Listed	StatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade Name: SafeDAY™
Generic Name: Basic intravenous administration set, noninvasive
Model / Ref / Catalog: 352646

Primary DI / UDI-DI: 04046955626946
FDA Product Code: FMG, FPA
GMDN Term: Basic intravenous administration set, noninvasive

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

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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