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BD Vacutainer® Serum 6.0mL

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® Serum 6.0mL FDA UDI
Generic Name
Evacuated blood collection tube IVD, clot activator/separator FDA UDI
Device Name
BD Vacutainer® Serum 6.0mL FDA UDI
Model / Reference
368044 FDA UDI
Description
BD Vacutainer® Serum 6.0mL FDA UDI

Identifiers

Catalog Number
368044 FDA UDI
Primary DI / UDI-DI
30382903680444 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Evacuated blood collection tube IVD, clot activator/separator 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

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: Evacuated blood collection tube IVD, clot activator/separator

BD Vacutainer® Serum 6.0mL by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Evacuated blood collection tube IVD, clot activator/separator.

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 2cee8db5-5181-4e91-8eeb-b36a7b740581 35 fields · synced May 30, 2026