Duns Number:012430880
Device Description: FX-57 Vinyl Packet Size 2
Catalog Number
1125333
Brand Name
Henry Schein
Version/Model Number
1125333
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
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
IWZ
Product Code Name
Film, radiographic
Public Device Record Key
b0406aa3-b57d-4b03-96fc-7ad664f57162
Public Version Date
April 11, 2019
Public Version Number
1
DI Record Publish Date
April 03, 2019
Package DI Number
20304040041011
Quantity per Package
50
Contains DI Package
10304040041014
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
1125333
| 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 |