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MaxGuard MX4470

by BD Switzerland Sàrl

MaxGuard MX4470 is a Class II device made by BD Switzerland Sàrl, listed in FDA GUDID since 22 Sep 2016 (UDI-DI 10885403241925), 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 Number10885403241925 UDI-DI Date22 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  • Withdrawn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
MaxGuard
Generic name
Basic intravenous administration set, noninvasive
Model / Ref / Catalog
MX4470
Primary DI / UDI-DI
10885403241925
FDA product code
FPA
GMDN term
Basic intravenous administration set, noninvasive
Device class
Class II
Regulation number
880.5440
GUDID distribution status
In Commercial Distribution

Related devices

Category: Basic intravenous administration set, noninvasive

Other devices from BD Switzerland Sàrl

See all devices from BD Switzerland Sàrl →

Properties

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