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BD Perisafe, BD

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Perisafe, BD FDA UDI
Generic Name
Luer/epidural catheter linear connector FDA UDI
Device Name
CATHETER W/CONN S/SU 20GA CE FOR 3-1/2IN FDA UDI
Model / Reference
400507 FDA UDI
Description
CATHETER W/CONN S/SU 20GA CE FOR 3-1/2IN FDA UDI

Identifiers

Catalog Number
400507 FDA UDI
Primary DI / UDI-DI
00382904005078 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Luer/epidural catheter linear connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
868.5140 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Needle Gauge — 20 Gauge FDA UDI
Length — 36 Inch FDA UDI

Category: Luer/epidural catheter linear connector

BD Perisafe, BD by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer/epidural catheter linear connector.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Becton Dickinson And Company

Sources (1)

  • FDA UDI e72f25e4-ec51-4c32-9520-f3d3f70bbf4d 35 fields · synced Jun 8, 2026