Duns Number:622223196
Device Description: BD 115 = 960 TestsBD 115/120 = 120 Tests
Catalog Number
BD 115, BD 115/120
Brand Name
SteriTec Green Card Bowie-Dick Test
Version/Model Number
BD 115
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"
-
For Single-Use
Yes
Prescription Use (Rx)
-
Over the Counter (OTC)
-
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
JOJ
Product Code Name
Indicator, Physical/Chemical Sterilization Process
Public Device Record Key
678658f9-71c9-4298-b1b8-7303caa79b64
Public Version Date
February 19, 2021
Public Version Number
3
DI Record Publish Date
September 23, 2016
Package DI Number
30814434020029
Quantity per Package
8
Contains DI Package
20814434020022
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Carton
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 61 |