BD Nexiva

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name: BD Nexiva FDA UDI
Generic Name: Peripheral intravenous cannula FDA UDI
Device Name: Nexiva 22Gx1.75” Dual Port MaxZero Cue FDA UDI
Model / Reference: 393553 FDA UDI
Description: Nexiva 22Gx1.75” Dual Port MaxZero Cue FDA UDI

Identifiers

Catalog Number: 393553 FDA UDI
Primary DI / UDI-DI: 00801741222887 FDA UDI
FDA Product Code: FPA FDA UDI
FOZ FDA UDI
GMDN Term: Peripheral intravenous cannula FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
880.5200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Dimensions & Sizes

Size: Length — 1.75 Inch FDA UDI
Needle Gauge — 22 Gauge FDA UDI

Category: Peripheral intravenous cannula

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

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Becton Dickinson And Company

Sources (1)

FDA UDI e2e4f489-74ea-4a8e-bc5c-290ba0715be8 36 fields · synced Jun 8, 2026