Duns Number:068199363
Device Description: Adult Bite Block
Catalog Number
100411
Brand Name
Adult Bite Block
Version/Model Number
100411
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
May 25, 2022
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)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MNK
Product Code Name
Endoscopic Bite Block
Public Device Record Key
d1949c69-d613-4065-9fd3-44bf38d24e49
Public Version Date
May 26, 2022
Public Version Number
4
DI Record Publish Date
March 19, 2021
Package DI Number
10677964060684
Quantity per Package
50
Contains DI Package
00677964060687
Package Discontinue Date
May 25, 2022
Package Status
Not in Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 2999 |
2 | A medical device with a moderate to high risk that requires special controls. | 362 |