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BD MiniDraw™ Capillary Tube Adapter H&H

FDA UDI

Class II (US FDA UDI)

by Becton Dickinson And Company

Identity

Trade Name
BD MiniDraw™ Capillary Tube Adapter H&H FDA UDI
Generic Name
Instrument/analyser test tube rack adaptor IVD FDA UDI
Device Name
BD MiniDraw™ Capillary Tube Adapter H&H FDA UDI
Model / Reference
366619 FDA UDI
Description
BD MiniDraw™ Capillary Tube Adapter H&H FDA UDI

Identifiers

Catalog Number
366619 FDA UDI
Primary DI / UDI-DI
50382903666190 FDA UDI
510(k) Number
K230493 FDA UDI
FDA Product Code
GIM FDA UDI
GMDN Term
Instrument/analyser test tube rack adaptor IVD 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

No

FDA UDI

Single Use

No

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

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Instrument/analyser test tube rack adaptor IVD

BD MiniDraw™ Capillary Tube Adapter H&H by Becton Dickinson And Company — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Cleared under the same submission

K230493 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 e802f7a6-34d2-4b94-81db-ba8c18bde31c 36 fields · synced May 30, 2026