Duns Number:342243334
Device Description: Cysto.-Urethro.-sheath,compl.,19Ch.
Catalog Number
35.007.05
Brand Name
Cysto.-Urethro.-sheath,compl.,19Ch.
Version/Model Number
35.007.05
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
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
-
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
JFL
Product Code Name
PH RATE MEASUREMENT, CARBON-DIOXIDE
Public Device Record Key
9449dfdc-8064-4e49-9a38-3e59d3eab83e
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 03, 2016
Package DI Number
EMAH35007051
Quantity per Package
1
Contains DI Package
EMAH35007050
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 19 |
2 | A medical device with a moderate to high risk that requires special controls. | 1976 |