PIVO™ Pro Needle-free Blood Collection Device

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name: PIVO™ Pro Needle-free Blood Collection Device FDA UDI
Generic Name: Blood transfer set FDA UDI
Device Name: PIVO™ Pro Needle-free Blood Collection Device 22 GA Compatible FDA UDI
Model / Reference: 393653 FDA UDI
Description: PIVO™ Pro Needle-free Blood Collection Device 22 GA Compatible FDA UDI

Identifiers

Catalog Number: 393653 FDA UDI
Primary DI / UDI-DI: 00382903936533 FDA UDI
FDA Product Code: JKA FDA UDI
GMDN Term: Blood transfer set FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 862.1675 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

Yes

FDA UDI

Category: Blood transfer set

PIVO™ Pro Needle-free Blood Collection Device 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 5ddebd05-f9c6-411f-a0b9-a74e0469baec 35 fields · synced May 30, 2026