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QuickSlide™

FDA UDI

Class I (US FDA UDI)

by Hardy Diagnostics

Identity

Trade Name
QuickSlide™ FDA UDI
Generic Name
Microscope slide stainer IVD FDA UDI
Device Name
GramPRO 3, Automated Gram Stain Instrument. Intended to be used to perform a Gram stain sequence on slides containing biological specimens in preparation for subsequent microscopic analysis. For in vitro diagnostic use. FDA UDI
Model / Reference
GP3 FDA UDI
Description
GramPRO 3, Automated Gram Stain Instrument. Intended to be used to perform a Gram stain sequence on slides containing biological specimens in preparation for subsequent microscopic analysis. For in vitro diagnostic use. FDA UDI

Identifiers

Catalog Number
GP3 FDA UDI
Primary DI / UDI-DI
00816576023998 FDA UDI
FDA Product Code
KPA FDA UDI
GMDN Term
Microscope slide stainer IVD FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.3800 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

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: Microscope slide stainer IVD

QuickSlide™ by Hardy Diagnostics — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microscope slide stainer IVD.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Hardy Diagnostics

Sources (1)

  • FDA UDI cfe6ae22-e91c-4200-97ec-ded4b9678c44 35 fields · synced May 29, 2026