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HHV-6 IgG Sera Pack

FDA UDI

Class I (US FDA UDI)

by Gold Standard Diagnostics, LLC

Identity

Trade Name
HHV-6 IgG Sera Pack FDA UDI
Generic Name
Assay development analyte-specific reagent IVD FDA UDI
Device Name
HHV-6 IgG Sera Pack FDA UDI
Model / Reference
GSD05-1700-SP FDA UDI
Description
HHV-6 IgG Sera Pack FDA UDI

Identifiers

Catalog Number
GSD05-1700-SP FDA UDI
Primary DI / UDI-DI
B350GSD051700SP0 FDA UDI
FDA Product Code
MVU FDA UDI
GMDN Term
Assay development analyte-specific reagent IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.4020 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

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assay development analyte-specific reagent IVD

HHV-6 IgG Sera Pack by Gold Standard Diagnostics, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Assay development analyte-specific reagent IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 835c03b7-aaf2-4a45-a2ea-b795a0d36329 35 fields · synced Jun 8, 2026