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BD Durasafe Plus, BD Epilor

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Durasafe Plus, BD Epilor FDA UDI
Generic Name
Epidural anaesthesia set, non-medicated FDA UDI
Device Name
DURASAFE+EL CSE M-KIT 27G WHX18G WS PLOR FDA UDI
Model / Reference
400287 FDA UDI
Description
DURASAFE+EL CSE M-KIT 27G WHX18G WS PLOR FDA UDI

Identifiers

Catalog Number
400287 FDA UDI
Primary DI / UDI-DI
00382904002879 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Epidural 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

No

FDA UDI

Combination Product

No

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 anaesthesia set, non-medicated

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

Similar devices

Also classified as Epidural anaesthesia set, non-medicated.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d5748755-f25b-4b4d-9f2f-4efbd88aa42a 34 fields · synced Jun 1, 2026