Steripath Micro

FDA UDI

Class II (US FDA UDI)

by Magnolia Medical Technologies, Inc.

Identity

Trade Name: Steripath Micro FDA UDI
Generic Name: Blood collection set, noninvasive FDA UDI
Device Name: SteriPath Micro, Luer, 10ml FDA UDI
Model / Reference: 4010-EN FDA UDI
Description: SteriPath Micro, Luer, 10ml FDA UDI

Identifiers

Catalog Number: 4010-EN FDA UDI
Primary DI / UDI-DI: 00858366007443 FDA UDI
FDA Product Code: JKA FDA UDI
FPA FDA UDI
GMDN Term: Blood collection set, noninvasive FDA UDI

Classification

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Blood transfer set Blood collection set, noninvasive

Steripath Micro by Magnolia Medical Technologies, Inc. — Class II — 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 II	Pending data

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Manufacturer

Manufacturer: Magnolia Medical Technologies, Inc.

Sources (1)

FDA UDI 7b7b612d-f0d4-47a7-b105-8b9055c20a10 34 fields · synced May 30, 2026