Duns Number:134472476
Catalog Number
335560REG
Brand Name
Regard™
Version/Model Number
C100AC-ZOLL
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
MLN
Product Code Name
Electrode, Electrodcardiograph, Multi-Function
Public Device Record Key
e74c22f4-56b8-4fd0-9d23-5c62fb8344c5
Public Version Date
September 02, 2020
Public Version Number
3
DI Record Publish Date
March 24, 2017
Package DI Number
10326053106009
Quantity per Package
10
Contains DI Package
20326053106006
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 305 |
2 | A medical device with a moderate to high risk that requires special controls. | 558 |