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BD Syringe NRFit™ Lok

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Syringe NRFit™ Lok FDA UDI
Generic Name
Neuraxial syringe FDA UDI
Device Name
BD® 20mL Syringe NRFit™ Lok FDA UDI
Model / Reference
400182 FDA UDI
Description
BD® 20mL Syringe NRFit™ Lok FDA UDI

Identifiers

Catalog Number
400182 FDA UDI
Primary DI / UDI-DI
00382904001827 FDA UDI
FDA Product Code
QEH FDA UDI
GMDN Term
Neuraxial syringe FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5860 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

Yes

FDA UDI

Dimensions & Sizes

Size
Total Volume — 20 Milliliter FDA UDI

Category: Neuraxial syringe

BD Syringe NRFit™ Lok by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Neuraxial syringe.

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 7fd24f30-efc5-4468-9162-e8ec03eca58d 36 fields · synced May 30, 2026