Duns Number:012430880
Device Description: AIR ANODIZED COMPOSIT INST. F5
Catalog Number
9008066
Brand Name
Henry Schein
Version/Model Number
9008066
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
EIY
Product Code Name
INSTRUMENT, FILLING, PLASTIC, DENTAL
Public Device Record Key
ba384d29-e5ff-4bd2-b1fc-2448d96bc3bd
Public Version Date
September 22, 2020
Public Version Number
2
DI Record Publish Date
August 24, 2020
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 | 3829 |
2 | A medical device with a moderate to high risk that requires special controls. | 2579 |
3 | A medical device with high risk that requires premarket approval | 1 |
U | Unclassified | 34 |