Duns Number:116903307
Device Description: MICROARCH® EURO/LP SNC 022 UL7-7 CS-BC HK
Catalog Number
K72-772-82
Brand Name
N/A
Version/Model Number
K72-772-82
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
February 19, 2021
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
-
Product Code
DZD
Product Code Name
TUBE, ORTHODONTIC
Public Device Record Key
ec84ba42-7dc7-4bc5-87c4-fa6bbbe49da6
Public Version Date
February 22, 2021
Public Version Number
3
DI Record Publish Date
August 30, 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 | 467 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 18 |