Duns Number:025460908
Device Description: THERMOMETER,DIGITAL,RECTAL,F/C,30 SEC
Catalog Number
MDS9952
Brand Name
Medline
Version/Model Number
MDS9952
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
Yes
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
K173113,K183431,K211931,K173113,K183431,K211931,K173113,K183431,K211931
Product Code
FLL
Product Code Name
Thermometer, electronic, clinical
Public Device Record Key
73f1b58a-c05e-4aad-b9e3-d445cf4d088b
Public Version Date
April 08, 2022
Public Version Number
1
DI Record Publish Date
March 31, 2022
Package DI Number
30888277116522
Quantity per Package
12
Contains DI Package
00888277116521
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 | 38540 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 85094 |
| 3 | A medical device with high risk that requires premarket approval | 2 |
| U | Unclassified | 7 |