Para-Pak SVT - Para-Pak SVT (Single Vial Transport) is a - MERIDIAN BIOSCIENCE, INC.

Duns Number:092815364

Device Description: Para-Pak SVT (Single Vial Transport) is a convenient one-vial system for the routine colle Para-Pak SVT (Single Vial Transport) is a convenient one-vial system for the routine collection, transportation, preservation and examination of stool specimens for intestinal parasites. Stool specimens preserved in Para-Pak SVT can be used for direct examination, concentration, permanent stain and in fecal immunoassays. The fixative affords an excellent means of minimizing the adverse effects of delay in specimen transport.

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More Product Details

Catalog Number

9016-01

Brand Name

Para-Pak SVT

Version/Model Number

9016-01

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

aad8febf-e8b4-4b0b-b9bc-f29e2152897b

Public Version Date

July 22, 2021

Public Version Number

2

DI Record Publish Date

July 06, 2021

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