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BD Vacutainer® Blood Alcohol Determinations Tube

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® Blood Alcohol Determinations Tube FDA UDI
Generic Name
Evacuated blood collection tube IVD, anticoagulant/antiglycolytic FDA UDI
Device Name
TUBE BAC GC 16X100 10.0 PLBL GR NAF/KOX FDA UDI
Model / Reference
367001 FDA UDI
Description
TUBE BAC GC 16X100 10.0 PLBL GR NAF/KOX FDA UDI

Identifiers

Catalog Number
367001 FDA UDI
Primary DI / UDI-DI
30382903670018 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Evacuated blood collection tube IVD, anticoagulant/antiglycolytic 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

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

Category: Evacuated blood collection tube IVD, anticoagulant/antiglycolytic

BD Vacutainer® Blood Alcohol Determinations Tube 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, anticoagulant/antiglycolytic.

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 28f4c8e1-2e2c-402e-b114-550425cefe1b 35 fields · synced May 30, 2026