Duns Number:961027315
Device Description: STETHOSCOPE ADULT DUAL HEAD PURPLE
Catalog Number
SMD21APR
Brand Name
CARDINAL HEALTH
Version/Model Number
SMD21APR
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 31, 2021
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
-
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
86b0b2b6-cd5f-4658-b1a7-0dc7fd5981f1
Public Version Date
December 31, 2021
Public Version Number
3
DI Record Publish Date
June 06, 2019
Package DI Number
10888499002043
Quantity per Package
10
Contains DI Package
00888499002046
Package Discontinue Date
December 31, 2021
Package Status
Not in Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 101686 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 139430 |
| 3 | A medical device with high risk that requires premarket approval | 8 |
| U | Unclassified | 40 |