Duns Number:315427286
Device Description: Safety module, medium tension to 6 N (600 g)
Catalog Number
-
Brand Name
N.A.
Version/Model Number
745-029-00
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
K936151,K936151
Product Code
DZB
Product Code Name
Headgear, extraoral, orthodontic
Public Device Record Key
ff9e1b19-219a-4417-95cc-3f812ecea38e
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 15, 2016
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 | 2768 |
2 | A medical device with a moderate to high risk that requires special controls. | 1745 |