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BD Perisafe, BD Epilor, BD Luer-Lok

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Perisafe, BD Epilor, BD Luer-Lok FDA UDI
Generic Name
Epidural/intrathecal anaesthesia set, non-medicated FDA UDI
Device Name
TRAY EPID CONT WE17G3.5 SWC X3800 FDA UDI
Model / Reference
406310 FDA UDI
Description
TRAY EPID CONT WE17G3.5 SWC X3800 FDA UDI

Identifiers

Catalog Number
406310 FDA UDI
Primary DI / UDI-DI
00382904063108 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Epidural/intrathecal anaesthesia set, non-medicated 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

Yes

FDA UDI

Combination Product

Yes

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Epidural/intrathecal anaesthesia set, non-medicated

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

Similar devices

Also classified as Epidural/intrathecal anaesthesia set, non-medicated.

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 e8c43220-80d2-4de8-bc0f-79835647f4d2 35 fields · synced May 30, 2026