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Negative Serum Control

FDA UDI

Class II (US FDA UDI)

by Immucor GTI Diagnostics, Inc.

Identity

Trade Name
Negative Serum Control FDA UDI
Generic Name
Platelet factor 4 IVD, control FDA UDI
Device Name
For Use with PF4 Enhanced (X-HAT13 & X-HAT45) and PF4 IgG (HAT13G & HAT45G) FDA UDI
Model / Reference
403623 FDA UDI
Description
For Use with PF4 Enhanced (X-HAT13 & X-HAT45) and PF4 IgG (HAT13G & HAT45G) FDA UDI

Identifiers

Catalog Number
403623 FDA UDI
Primary DI / UDI-DI
10888234500414 FDA UDI
FDA Product Code
LCO FDA UDI
GMDN Term
Platelet factor 4 IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
864.7695 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

No

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

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: Platelet factor 4 IVD, control

Negative Serum Control by Immucor GTI Diagnostics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Platelet factor 4 IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d458e0f0-7d25-46db-a6b7-8184d0b3ecb2 36 fields · synced May 29, 2026