Duns Number:002125419
Device Description: 26 in. (66 cm) - Blue Stripe
Catalog Number
-
Brand Name
BodyGuard BodySet
Version/Model Number
A120-160SAS
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
October 15, 2020
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)
Yes
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
d166d4c1-f4ef-4d40-9b88-a9d0db84593b
Public Version Date
November 16, 2020
Public Version Number
2
DI Record Publish Date
August 01, 2019
Package DI Number
10818666020433
Quantity per Package
50
Contains DI Package
00818666020436
Package Discontinue Date
October 15, 2020
Package Status
Not in Commercial Distribution
Package Type
Case
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 125 |