Duns Number:106712748
Catalog Number
-
Brand Name
Level 1
Version/Model Number
C203-10
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"
Yes
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
K912280,K912280
Product Code
FLL
Product Code Name
Thermometer, electronic, clinical
Public Device Record Key
93f3403e-5ca1-4376-a7ce-b9f4a1062e22
Public Version Date
August 17, 2018
Public Version Number
4
DI Record Publish Date
October 14, 2016
Package DI Number
30695085001526
Quantity per Package
100
Contains DI Package
20695085001529
Package Discontinue Date
-
Package Status
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 | 3 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 686 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 1 |