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McKesson

FDA UDI

Class II (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Microhaematocrit centrifuge IVD FDA UDI
Device Name
Centrifuge 6 Place Fixed Angle Rotor Variable Speed up to 4,000 RPM FDA UDI
Model / Reference
602 FDA UDI
Description
Centrifuge 6 Place Fixed Angle Rotor Variable Speed up to 4,000 RPM FDA UDI

Identifiers

Primary DI / UDI-DI
40612479200102 FDA UDI
FDA Product Code
GKG FDA UDI
GMDN Term
Microhaematocrit centrifuge IVD FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.6400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

Yes

FDA UDI

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Microhaematocrit centrifuge IVD

McKesson by Mckesson Medical-Surgical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microhaematocrit centrifuge IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e9948832-3853-4619-9b6b-543a579bb9e6 33 fields · synced May 30, 2026