Kbmed

FDA UDI

Class I (US FDA UDI)

by KB Medical (group), Inc.

Identity

Trade Name: KBMED FDA UDI
Generic Name: Blood collection tube holder, single-use FDA UDI
Device Name: Tube Holder, Pack of 200pcs FDA UDI
Model / Reference: NH01 FDA UDI
Description: Tube Holder, Pack of 200pcs FDA UDI

Identifiers

Primary DI / UDI-DI: 10850016172676 FDA UDI
FDA Product Code: KST FDA UDI
GMDN Term: Blood collection tube holder, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

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: Blood collection tube holder, single-use

Kbmed by KB Medical (group), Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Blood Collection Tube Holders — Dynarex Corp. · Class I
GCB Medical Supply — GCB MEDICAL LLC · Class II

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: KB Medical (group), Inc.

Sources (1)

FDA UDI d04c9154-cb6e-4503-8377-309415157fe9 33 fields · synced Jun 8, 2026