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BD Vacutainer® Luer-Lok™ Access Device

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Vacutainer® Luer-Lok™ Access Device FDA UDI
Generic Name
Luer-ended blood collection tube spike FDA UDI
Device Name
BD LUER-LOK ACCESS DEVICE FDA UDI
Model / Reference
36490200 FDA UDI
Description
BD LUER-LOK ACCESS DEVICE FDA UDI

Identifiers

Catalog Number
36490200 FDA UDI
Primary DI / UDI-DI
00382903649020 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Luer-ended blood collection tube spike 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: Luer-ended blood collection tube spike

BD Vacutainer® Luer-Lok™ Access Device by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Luer-ended blood collection tube spike.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6b859569-1828-47af-9563-8a6490e20a86 35 fields · synced Jun 8, 2026