Duns Number:942778564
Device Description: PROLUBE 100 BOX
Catalog Number
MCPLBOX100
Brand Name
ProLube
Version/Model Number
MCPLBOX100
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
EIC
Product Code Name
SYRINGE, PERIODONTIC, ENDODONTIC, IRRIGATING
Public Device Record Key
0f9c51ff-daa7-453f-9e86-6609f8ab87dd
Public Version Date
September 14, 2022
Public Version Number
1
DI Record Publish Date
September 06, 2022
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 | 1973 |
2 | A medical device with a moderate to high risk that requires special controls. | 35 |
U | Unclassified | 16 |