Duns Number:005473608
Device Description: GC Tri Plaque ID Gel™ 40g tube (36 mL, approximately 130 applications)
Catalog Number
004273
Brand Name
GC Tri Plaque ID Gel™
Version/Model Number
004273
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
August 06, 2016
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
-
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
NYH
Product Code Name
plaque disclosing kit
Public Device Record Key
6c322195-34b3-4301-8e8a-1a8379691ce2
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 01, 2016
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 | 480 |
2 | A medical device with a moderate to high risk that requires special controls. | 4772 |