Duns Number:828918164
Device Description: Sterile Lubricating Jelly, Packet
Catalog Number
211
Brand Name
HR Lubricating Jelly 2X
Version/Model Number
211
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"
Yes
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
KMJ
Product Code Name
Lubricant, patient
Public Device Record Key
48b92272-7f63-4201-95ff-11f00c655979
Public Version Date
September 27, 2018
Public Version Number
1
DI Record Publish Date
August 27, 2018
Package DI Number
50851809002116
Quantity per Package
576
Contains DI Package
00851809002111
Package Discontinue Date
-
Package Status
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 | 16 |
2 | A medical device with a moderate to high risk that requires special controls. | 66 |