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McKesson

FDA UDI

Class I (US FDA UDI)

by Mckesson Medical-Surgical Inc.

Identity

Trade Name
McKesson FDA UDI
Generic Name
Total human chorionic gonadotropin IVD, control FDA UDI
Device Name
CONTROL KIT, PREG HCG (1/BX) FDA UDI
Model / Reference
5011 FDA UDI
Description
CONTROL KIT, PREG HCG (1/BX) FDA UDI

Identifiers

Primary DI / UDI-DI
00612479202788 FDA UDI
FDA Product Code
JJX FDA UDI
GMDN Term
Total human chorionic gonadotropin IVD, control FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
862.1660 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

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Total human chorionic gonadotropin IVD, control

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

Similar devices

Also classified as Total human chorionic gonadotropin IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c02c95cc-8c0c-41fc-be20-0d4b9841ad2e 33 fields · synced Jun 8, 2026