Duns Number:342243334
Device Description: Resectoscope sheath-interior tube only, rotatable,26Ch.
Catalog Number
36.006.02RQL
Brand Name
Resectoscope sheath-interior tube only, rotatable,26Ch.
Version/Model Number
36.006.02RQL
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
Yes
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
34a5663d-4b9d-49a1-8700-9560c2b23f3a
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
August 03, 2016
Package DI Number
EMAH3600602RQL1
Quantity per Package
1
Contains DI Package
EMAH3600602RQL0
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 |