Duns Number:606939072
Device Description: Mr. Clear Purple No Foam Pad
Catalog Number
0600-AF031-NF-000
Brand Name
Mr. Clear Purple
Version/Model Number
0600-AF031-NF-000
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
January 10, 2020
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"
Yes
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
OCT
Product Code Name
Anti fog solution and accessories, endoscopy
Public Device Record Key
543fbb48-d412-4960-b4e6-7912d4e94d0a
Public Version Date
January 13, 2020
Public Version Number
2
DI Record Publish Date
January 24, 2019
Package DI Number
20817984010949
Quantity per Package
25
Contains DI Package
00817984010945
Package Discontinue Date
January 10, 2020
Package Status
Not in Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 37 |
2 | A medical device with a moderate to high risk that requires special controls. | 57 |