Duns Number:945020902
Catalog Number
-
Brand Name
Regard™
Version/Model Number
GS0366
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 25, 2020
Issuing Agency
In GS1
MRI safety Status
MR Safe
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
OHD
Product Code Name
Gynecological Laparoscopic Kit
Public Device Record Key
179068fd-6db4-4138-98a0-1a2783b0643a
Public Version Date
August 26, 2020
Public Version Number
3
DI Record Publish Date
December 05, 2016
Package DI Number
20326053106983
Quantity per Package
2
Contains DI Package
10326053106986
Package Discontinue Date
August 25, 2020
Package Status
Not 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 |