Duns Number:002111896
Device Description: Din Lead Wire, Snap to Socket, 24", 3 Lead Set
Catalog Number
20900-24-3A
Brand Name
Vermed
Version/Model Number
20900-24-3A
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In GS1
MRI safety Status
MR Unsafe
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)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K942321,K942321
Product Code
DSA
Product Code Name
Cable, Transducer And Electrode, Patient, (Including Connector)
Public Device Record Key
005a374e-7193-4c6d-af6b-b6c4a59814a5
Public Version Date
January 03, 2022
Public Version Number
2
DI Record Publish Date
September 28, 2018
Package DI Number
30009336008255
Quantity per Package
10
Contains DI Package
00009336008254
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Bag
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 161 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 269 |
| 3 | A medical device with high risk that requires premarket approval | 1 |