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BD Vacutainer® Specimen Collection with BD™ Blunt Plastic Cannula

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® Specimen Collection with BD™ Blunt Plastic Cannula FDA UDI
Generic Name
Luer-ended blood collection tube spike FDA UDI
Device Name
BD Vacutainer® Specimen Collection Assembly with BD™ Blunt Plastic Cannula FDA UDI
Model / Reference
303380 FDA UDI
Description
BD Vacutainer® Specimen Collection Assembly with BD™ Blunt Plastic Cannula FDA UDI

Identifiers

Catalog Number
303380 FDA UDI
Primary DI / UDI-DI
30382903033806 FDA UDI
510(k) Number
K974363 FDA UDI
FDA Product Code
FMI FDA UDI
GMDN Term
Luer-ended blood collection tube spike FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
880.5570 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: Luer-ended blood collection tube spike

BD Vacutainer® Specimen Collection with BD™ Blunt Plastic Cannula by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Luer-ended blood collection tube spike.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e6014c53-f262-4be4-8c30-070ad5cd1f2b 36 fields · synced May 30, 2026