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BD Microtainer® Tubes w/ FE (Sodium Fluoride/Disodium EDTA) Glycolytic Inhibitor

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD Microtainer® Tubes w/ FE (Sodium Fluoride/Disodium EDTA) Glycolytic Inhibitor FDA UDI
Generic Name
Non-evacuated blood collection tube IVD, anticoagulant/antiglycolytic FDA UDI
Device Name
BD Microtainer® Tubes with FE (Sodium Fluoride/Disodium EDTA) Glycolytic Inhibitor FDA UDI
Model / Reference
365992 FDA UDI
Description
BD Microtainer® Tubes with FE (Sodium Fluoride/Disodium EDTA) Glycolytic Inhibitor FDA UDI

Identifiers

Catalog Number
365992 FDA UDI
Primary DI / UDI-DI
30382903659921 FDA UDI
510(k) Number
K002456 FDA UDI
FDA Product Code
JKA FDA UDI
GMDN Term
Non-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

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/antiglycolytic

BD Microtainer® Tubes w/ FE (Sodium Fluoride/Disodium EDTA) Glycolytic Inhibitor 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/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 874059be-771e-4f5e-aaeb-acbf497ad379 36 fields · synced May 30, 2026