Duns Number:092815364
Device Description: This DI Number represents the DI number on the Inner Box. There are 20 individual vials pe This DI Number represents the DI number on the Inner Box. There are 20 individual vials per inner box. Para-Pak / Para-Pak Ultra based systems provide standardized procedures for the routine collection, transportation, preservation, and examination of stool specimens for intestinal parasites. Systems are designed for easy use by individuals not trained in microbiological procedures and afford an excellent means of minimizing the adverse effects of delay in specimen transportation.
Catalog Number
900112
Brand Name
Para-Pak LV-PVA
Version/Model Number
900112
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
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
IFQ
Product Code Name
Formulations, Mercuric Chloride For Tissue
Public Device Record Key
fde21b12-d785-4a23-b64e-c2a146c17750
Public Version Date
July 14, 2021
Public Version Number
1
DI Record Publish Date
July 06, 2021
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| 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 |