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BD Epilor

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Epilor FDA UDI
Generic Name
Low-resistance epidural syringe FDA UDI
Device Name
SYRINGE EPILOR PLASTIC LOR 7ML LS S/SU FDA UDI
Model / Reference
405292 FDA UDI
Description
SYRINGE EPILOR PLASTIC LOR 7ML LS S/SU FDA UDI

Identifiers

Catalog Number
405292 FDA UDI
Primary DI / UDI-DI
00382904052928 FDA UDI
510(k) Number
K210983 FDA UDI
FDA Product Code
CAZ FDA UDI
GMDN Term
Low-resistance epidural syringe 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

Category: Low-resistance epidural syringe

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

Similar devices

Also classified as Low-resistance epidural syringe.

Cleared under the same submission

K210983 also covers:

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 b650c9d8-6bc9-4b40-a60c-8c0e4c37f9c0 35 fields · synced May 30, 2026