Duns Number:071595540
Device Description: STIEGMANN-GOFF BANDITO Endoscopic Ligator, 40 Inch (102cm) Trip Wire
Catalog Number
100226
Brand Name
STIEGMANN-GOFF BANDITO
Version/Model Number
100226
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
June 06, 2022
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)
Yes
Device labeled as "Not made with natural rubber latex"
-
For Single-Use
Yes
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
MND
Product Code Name
Ligator, esophageal
Public Device Record Key
743afa08-92c0-43ac-88f5-33fdb6595ea1
Public Version Date
June 07, 2022
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
20653405053689
Quantity per Package
5
Contains DI Package
30653405053686
Package Discontinue Date
June 06, 2022
Package Status
Not in Commercial Distribution
Package Type
BOX
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 1412 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 2261 |
| 3 | A medical device with high risk that requires premarket approval | 95 |