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Steripath Micro

FDA UDI

Class II (US FDA UDI)

by Magnolia Medical Technologies, Inc.

Identity

Trade Name
Steripath Micro FDA UDI
Generic Name
Blood transfer set FDA UDI
Device Name
Steripath Micro, 21G UltraTouch, 10mL Syringe FDA UDI
Model / Reference
4010-21UT-EN FDA UDI
Description
Steripath Micro, 21G UltraTouch, 10mL Syringe FDA UDI

Identifiers

Catalog Number
4010-21UT-EN FDA UDI
Primary DI / UDI-DI
00858366007429 FDA UDI
FDA Product Code
FPA FDA UDI
JKA FDA UDI
GMDN Term
Blood transfer set 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

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Blood collection set, invasiveBlood transfer set

Steripath Micro by Magnolia Medical Technologies, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Blood transfer set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Magnolia Medical Technologies, Inc.

Sources (1)

  • FDA UDI c3c1475f-a2c2-45e0-83ea-ca2b47592fb0 34 fields · synced May 30, 2026