BD Vacutainer® Push Button Blood Collection Set

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name: BD Vacutainer® Push Button Blood Collection Set FDA UDI
Generic Name: Blood collection set, invasive FDA UDI
Device Name: BD Vacutainer® Push Button Blood Collection Set FDA UDI
Model / Reference: 367326 FDA UDI
Description: BD Vacutainer® Push Button Blood Collection Set FDA UDI

Identifiers

Catalog Number: 367326 FDA UDI
Primary DI / UDI-DI: 30382903673262 FDA UDI
510(k) Number: K220212 FDA UDI
FDA Product Code: FPA FDA UDI
JKA FDA UDI
GMDN Term: Blood collection set, invasive FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
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

FDA UDI

Category: Blood collection set, invasive

BD Vacutainer® Push Button Blood Collection Set by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Cleared under the same submission

K220212 also covers:

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 49bc3c95-f37e-4280-ac4e-0bae5b189f3a 36 fields · synced Jun 1, 2026