Duns Number:796452311
Device Description: DISP NLCR COMPAT SPO2 SNSR,OXMX,MAX-A
Catalog Number
26232
Brand Name
DISP NLCR COMPAT SPO2 SNSR,OXMX,MAX-A
Version/Model Number
CSA001DA-P200
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"
-
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
K182220,K182220
Product Code
DSA
Product Code Name
Cable, Transducer And Electrode, Patient, (Including Connector)
Public Device Record Key
7802b4a1-7ac9-4471-8104-56a85b25b14d
Public Version Date
November 10, 2021
Public Version Number
3
DI Record Publish Date
August 04, 2020
Package DI Number
10840828180563
Quantity per Package
30
Contains DI Package
00840828180566
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 478 |
2 | A medical device with a moderate to high risk that requires special controls. | 8062 |