Skip to content

BD Perisafe, BD 400507

by Becton, Dickinson and Company

BD Perisafe, BD 400507 is a Class II device made by Becton, Dickinson and Company, listed in FDA GUDID since 16 Sep 2016 (UDI-DI 00382904005078), registry data as of 26 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 26 Oct 2026.

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00382904005078 UDI-DI Date16 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  • Withdrawn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
BD Perisafe, BD
Generic name
Luer/epidural catheter linear connector
Model / Ref / Catalog
400507
Primary DI / UDI-DI
00382904005078
FDA product code
CAZ
GMDN term
Luer/epidural catheter linear connector
Device class
Class II
Regulation number
868.5140
GUDID distribution status
In Commercial Distribution
Size
Needle Gauge — 20 Gauge
Length — 36 Inch

Similar devices

Other devices filed under FDA product code CAZ (Anesthesia conduction kit).

Other devices from Becton, Dickinson and Company

See all devices from Becton, Dickinson and Company →

Properties

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