Hummi Micro-Draw

FDA UDI

Class I (US FDA UDI)

by Kentec Medical, Inc.

Identity

Trade Name: Hummi Micro-Draw FDA UDI
Generic Name: Arterial blood sampling kit FDA UDI
Device Name: hummi micro draw FDA UDI
Model / Reference: ABG-HM-1 FDA UDI
Description: hummi micro draw FDA UDI

Identifiers

Catalog Number: ABG-HM-1 FDA UDI
Primary DI / UDI-DI: 10817522013305 FDA UDI
FDA Product Code: KST FDA UDI
GMDN Term: Arterial blood sampling kit FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 864.9125 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Arterial blood sampling kit

Hummi Micro-Draw by Kentec Medical, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Kentec Medical, Inc.

Sources (1)

FDA UDI e31b36f9-47c6-444c-9921-fdf021867e2e 35 fields · synced May 30, 2026