Duns Number:008965063
Device Description: Piezo-electric stimulator for temporary reduction of itching and swelling resulting from m Piezo-electric stimulator for temporary reduction of itching and swelling resulting from mosquito bites
Catalog Number
-
Brand Name
Walgreens
Version/Model Number
Bite Relief
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
OSG
Product Code Name
Piezo-Electric Stimulator For Relief Of Mosquito Bite Itch
Public Device Record Key
e728c52d-e881-4018-be22-a959aca53311
Public Version Date
August 20, 2020
Public Version Number
2
DI Record Publish Date
December 21, 2018
Package DI Number
10311917206728
Quantity per Package
384
Contains DI Package
00311917206721
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
case pack
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 75 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 74 |
| U | Unclassified | 2 |