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Medical Action Industries

FDA UDI

Class I (US FDA UDI)

by Medical Action Industries Inc.

Identity

Trade Name
Medical Action Industries FDA UDI
Generic Name
Phlebotomy kit FDA UDI
Device Name
Kit: STB w/Vacutainer 50/Cs FDA UDI
Model / Reference
58400 FDA UDI
Description
Kit: STB w/Vacutainer 50/Cs FDA UDI

Identifiers

Primary DI / UDI-DI
10809160008386 FDA UDI
FDA Product Code
OFZ FDA UDI
GMDN Term
Phlebotomy kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.1100 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Phlebotomy kit

Medical Action Industries by Medical Action Industries Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Phlebotomy kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 5d19bf2e-02dd-4628-9689-6181eb53bed3 34 fields · synced Jun 6, 2026