Duns Number:315304071
Device Description: PROCTOSCOPE TUBE Ø 18.5MM WL 120MM WL 120mm, TL 135mm, slanted, reusable
Catalog Number
8836.035
Brand Name
NA
Version/Model Number
8836035
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
-
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
GCM
Product Code Name
ENDOSCOPE, RIGID
Public Device Record Key
b52af077-393f-4fc8-ae36-651f5cb29748
Public Version Date
March 29, 2018
Public Version Number
2
DI Record Publish Date
September 26, 2016
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
1 | A medical device with low to moderate risk that requires general controls | 587 |
2 | A medical device with a moderate to high risk that requires special controls. | 1835 |