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Crystal Violet

FDA UDI

Class I (US FDA UDI)

by Pro-Lab, Incorporated

Identity

Trade Name
Crystal Violet FDA UDI
Generic Name
Gram stain IVD, reagent FDA UDI
Device Name
For use in the Gram’s Staining method for the initial differentiation of Gram Positive and Gram Negative bacteria. FDA UDI
Model / Reference
PL.8000 FDA UDI
Description
For use in the Gram’s Staining method for the initial differentiation of Gram Positive and Gram Negative bacteria. FDA UDI

Identifiers

Catalog Number
PL.8000 FDA UDI
Primary DI / UDI-DI
05060472461421 FDA UDI
FDA Product Code
ICF FDA UDI
GMDN Term
Gram stain IVD, reagent FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
864.1850 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: Gram stain IVD, reagent

Crystal Violet by Pro-Lab, Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Gram stain IVD, reagent.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c860fbb2-7850-493e-b7d5-75673a86627d 34 fields · synced May 30, 2026