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BD Vacutainer&#174 - BD Vacutainer&#174

FDA UDI

Class I (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® No Additive (Z) FDA UDI
Generic Name
Evacuated blood collection tube IVD, no additive FDA UDI
Device Name
BD Vacutainer® No Additive (Z) FDA UDI
Model / Reference
366797 FDA UDI
Description
BD Vacutainer® No Additive (Z) FDA UDI

Identifiers

Catalog Number
366797 FDA UDI
Primary DI / UDI-DI
50382903667975 FDA UDI
FDA Product Code
FMH FDA UDI
GMDN Term
Evacuated blood collection tube IVD, no additive FDA UDI
Models / Variants
BD Vacutainer&#174 FDA UDI
No Additive (Z) FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3250 FDA UDI
Commercial Distribution
Not 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

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

BD Vacutainer&#174 - BD Vacutainer&#174 by Becton Dickinson And Company — Class I — FDA UDI — listed in FDA GUDID — 2 models — regulatory data on deviCERTS

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 02e585c7-26e4-4bdb-b039-405bbc643cc3 35 fields · synced May 30, 2026