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Ultraplex 360® 333630

by B. Braun Medical, Inc.

Ultraplex 360® 333630 is a Class II device made by B. Braun Medical, Inc., listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04046964726675), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04046964726675 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  • Withdrawn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
Ultraplex 360®
Generic name
Peripheral nerve-block blunt needle
Model / Ref / Catalog
333630
Primary DI / UDI-DI
04046964726675
FDA product code
BSP
GMDN term
Peripheral nerve-block blunt needle
Device class
Class II
Regulation number
868.5150
GUDID distribution status
In Commercial Distribution

Related devices

Category: Peripheral nerve-block blunt needle

Similar devices

Other devices filed under FDA product code BSP (NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)).

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)