Duns Number:006261481
Device Description: CONN PROBE CB4627 BIOACT FLOW PEDIATRIC
Catalog Number
-
Brand Name
Bio-Probe®
Version/Model Number
CB4627
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
November 30, 2017
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
Yes
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
K830858,K830858
Product Code
DPT
Product Code Name
PROBE, BLOOD-FLOW, EXTRAVASCULAR
Public Device Record Key
ddebdaf5-01a6-4f3b-bac6-7277f831f206
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
June 16, 2016
Package DI Number
20673978563330
Quantity per Package
10
Contains DI Package
00673978563336
Package Discontinue Date
November 30, 2017
Package Status
Not in Commercial Distribution
Package Type
PK
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 102 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 20495 |
| 3 | A medical device with high risk that requires premarket approval | 3601 |