Duns Number:121622872
Device Description: MC-RAN-11C-MAXX REGENPN 74292-01MCustomer# 0018407
Catalog Number
RB-REG-1
Brand Name
MC-RAN-11C
Version/Model Number
11GA X 9CM
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K150563,K150563,K150563
Product Code
KNW
Product Code Name
Instrument, Biopsy
Public Device Record Key
a02e7a39-8dad-4c72-bffd-ae636e0dfe14
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
May 09, 2017
Package DI Number
10858690006218
Quantity per Package
1
Contains DI Package
00858690006211
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Inner pack
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 31 |
2 | A medical device with a moderate to high risk that requires special controls. | 93 |