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Prolex L. pneumophila Serogroup 1 Positive Control Latex Reagent

FDA UDI

Class II (US FDA UDI)

by Pro-Lab, Incorporated

Identity

Trade Name
Prolex L. pneumophila Serogroup 1 Positive Control Latex Reagent FDA UDI
Generic Name
Legionella pneumophila nucleic acid IVD, control FDA UDI
Device Name
Prolex L. pneumophila Serogroup 1 Positive Control Latex Reagent FDA UDI
Model / Reference
PL.382 FDA UDI
Description
Prolex L. pneumophila Serogroup 1 Positive Control Latex Reagent FDA UDI

Identifiers

Catalog Number
PL.382 FDA UDI
Primary DI / UDI-DI
10628429002121 FDA UDI
FDA Product Code
LHL FDA UDI
GMDN Term
Legionella pneumophila nucleic acid IVD, control FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
866.3300 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: Legionella pneumophila nucleic acid IVD, control

Prolex L. pneumophila Serogroup 1 Positive Control Latex Reagent by Pro-Lab, Incorporated — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Legionella pneumophila nucleic acid IVD, control.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pro-Lab, Incorporated

Sources (1)

  • FDA UDI 659d1238-6dbb-4ef8-b8da-da555af41fe4 34 fields · synced May 30, 2026