Duns Number:791014871
Device Description: BP Kit, 22"Sprague, Light Blue
Catalog Number
2080LB
Brand Name
Tech-Med
Version/Model Number
2080LB
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 13, 2018
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"
-
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
K780715,K780715
Product Code
DXQ
Product Code Name
blood pressure cuff
Public Device Record Key
4a0739b2-3669-4fd8-905c-5dd79244e66f
Public Version Date
May 23, 2022
Public Version Number
6
DI Record Publish Date
September 24, 2016
Package DI Number
20665973016881
Quantity per Package
24
Contains DI Package
00665973016887
Package Discontinue Date
June 13, 2018
Package Status
Not 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 | 2 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 31 |
| U | Unclassified | 1 |