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Multi-Ad® 513548

by B. Braun Medical, Inc.

Multi-Ad® 513548 is a Class I device made by B. Braun Medical, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04022495818348), registry data as of 23 Oct 2026.

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

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04022495818348 UDI-DI Date23 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Multi-Ad®
Generic name
Pharmaceutical fluid-dispensing system
Model / Ref / Catalog
513548
Primary DI / UDI-DI
04022495818348
FDA product code
KYX
GMDN term
Pharmaceutical fluid-dispensing system
Device class
Class I
Regulation number
880.6430
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pharmaceutical fluid-dispensing system

Similar devices

Other devices filed under FDA product code KYX (DISPENSER, LIQUID MEDICATION).

Other devices from B. Braun Medical, Inc.

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

Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (10, all answered No)