Para-Pak EcoFix - Para-Pak/Para-Pak ULTRA EcoFix is a convenient - MERIDIAN BIOSCIENCE, INC.

Duns Number:092815364

Device Description: Para-Pak/Para-Pak ULTRA EcoFix is a convenient one-vial system for the routine collection, Para-Pak/Para-Pak ULTRA EcoFix is a convenient one-vial system for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. Both concentration and permanent stain may be performed from the EcoFix preserved specimen. The fixative affords an excellent means of minimizing the adverse effects of delay in specimen transport.Primary DI Number 00840733102400 indicates the innerbox of the device.

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More Product Details

Catalog Number

901312

Brand Name

Para-Pak EcoFix

Version/Model Number

901312

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

LDX

Product Code Name

Fixative, Metallic Containing

Device Record Status

Public Device Record Key

0d5ba8d0-12f1-4e1e-bef7-b2dcd02e067e

Public Version Date

March 22, 2022

Public Version Number

3

DI Record Publish Date

December 09, 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