Duns Number:001661222
Device Description: BIA SCALE
Catalog Number
-
Brand Name
CONAIR COPORATION
Version/Model Number
WW712XF
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 22, 2019
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
MNW
Product Code Name
Analyzer, Body Composition
Public Device Record Key
bd1edf04-a7af-41ef-ab3a-ca8e076ffbef
Public Version Date
May 30, 2019
Public Version Number
1
DI Record Publish Date
May 22, 2019
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 | 132 |
2 | A medical device with a moderate to high risk that requires special controls. | 62 |