Para-Pak Ultra EcoFix / C&S / Clean - Para-Pak systems are convenient system for the - MERIDIAN BIOSCIENCE, INC.

Duns Number:092815364

Device Description: Para-Pak systems are convenient system for the routine collection, transportation, preserv Para-Pak systems are convenient system for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. The systems are designed for easy collection of specimens by individuals not trained in microbiological techniques and affords and excellent means of minimizing the adverse effects of delay in specimen transport.

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More Product Details

Catalog Number

331612

Brand Name

Para-Pak Ultra EcoFix / C&S / Clean

Version/Model Number

331612

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

Yes

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code Details

Product Code

FMH

Product Code Name

Container, Specimen, Sterile

Device Record Status

Public Device Record Key

90974b21-aa12-4875-b37c-1243ecc728aa

Public Version Date

July 22, 2021

Public Version Number

2

DI Record Publish Date

December 10, 2020

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"MERIDIAN BIOSCIENCE, INC." Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 149
2 A medical device with a moderate to high risk that requires special controls. 46
3 A medical device with high risk that requires premarket approval 1