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BD Microtainer® PST™ Tubes with LH (Lithium Heparin) - Amber

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Microtainer® PST™ Tubes with LH (Lithium Heparin) - Amber FDA UDI
Generic Name
Non-evacuated blood collection tube IVD, anticoagulant/separator FDA UDI
Device Name
TUBE MICRO W/MICROGARD PST MTGN/AMB FDA UDI
Model / Reference
365987 FDA UDI
Description
TUBE MICRO W/MICROGARD PST MTGN/AMB FDA UDI

Identifiers

Catalog Number
365987 FDA UDI
Primary DI / UDI-DI
30382903659877 FDA UDI
510(k) Number
K991702 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Non-evacuated blood collection tube IVD, anticoagulant/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: Non-evacuated blood collection tube IVD, anticoagulant/separator

BD Microtainer® PST™ Tubes with LH (Lithium Heparin) - Amber by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Non-evacuated blood collection tube IVD, anticoagulant/separator.

Cleared under the same submission

K991702 also covers:

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 08144cef-b507-4b2e-8a19-7c50bf1c92c5 36 fields · synced May 31, 2026