Kbmed

FDA UDI

Class II (US FDA UDI)

by KB Medical (group), Inc.

Identity

Trade Name: KBMED FDA UDI
Generic Name: Blood collection set, invasive FDA UDI
Device Name: PUSH BUTTON SAFETY BLOOD COLLECTION SET, 25G*3/4" with 12" tubing, box of 50pcs FDA UDI
Model / Reference: SBCNP25K-1 FDA UDI
Description: PUSH BUTTON SAFETY BLOOD COLLECTION SET, 25G*3/4" with 12" tubing, box of 50pcs FDA UDI

Identifiers

Primary DI / UDI-DI: 10810100051256 FDA UDI
FDA Product Code: FPA FDA UDI
JKA FDA UDI
GMDN Term: Blood collection set, invasive FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5440 FDA UDI
862.1675 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

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Blood collection set, invasive

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

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Also classified as Blood collection set, invasive.

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SteriPath Gen2, 23G, BD — MAGNOLIA MEDICAL TECHNOLOGIES, INC. · Class II
RELI® — MYCO MEDICAL SUPPLIES INC. · Class II
Kawasumi — Jiangsu Caina Medical Co., Ltd · Class II
Custom Healthcare Systems Inc. — Manus Medical, LLC

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 II	Pending data

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Manufacturer

Manufacturer: KB Medical (group), Inc.

Sources (1)

FDA UDI 39ccb56c-ab2b-46c4-914e-20f8f4869170 33 fields · synced May 30, 2026