Duns Number:108999095
Device Description: Scope ID Tag, Engravable,Black
Catalog Number
697BKL
Brand Name
Adscope®
Version/Model Number
697BKL
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
LDE
Product Code Name
Stethoscope, Manual
Public Device Record Key
8c2ccf28-6421-4380-a5f3-8a25b8e5ed34
Public Version Date
November 02, 2020
Public Version Number
1
DI Record Publish Date
October 24, 2020
Package DI Number
00634782899875
Quantity per Package
10
Contains DI Package
00634782098483
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 | 2395 |
2 | A medical device with a moderate to high risk that requires special controls. | 1769 |