Duns Number:989586482
Device Description: This device is intended for use as an endoscopic instrument(s) and/or camera port during m This device is intended for use as an endoscopic instrument(s) and/or camera port during minimally invasive abdominal surgery.The ASC TriPort+ is a sterile, disposable endoscopic multi-instrument port. The device consists of the following:• An Introducer that allows the insertion of the Base Retractor into the abdomen through an incision.• A Base Retractor that retracts in an abdominal incision to allow laparoscopic instruments pass through to the abdomen. • A Boot contains four instrument valves and two ports that allow insufflation of the abdomen or venting of electrocautery gases. The Boot maintains pneumoperitoneum when attached and allows specimen removal when detached.
Catalog Number
-
Brand Name
TriPort+
Version/Model Number
WA58010T
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"
Yes
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
K110004,K110004
Product Code
GCJ
Product Code Name
Laparoscope, General & Plastic Surgery
Public Device Record Key
f6f5d140-0aa9-4464-a454-8ef5488dabc8
Public Version Date
July 06, 2018
Public Version Number
3
DI Record Publish Date
September 13, 2016
Package DI Number
05391530440066
Quantity per Package
5
Contains DI Package
05391530440073
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CARTON OF 5
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 2 | A medical device with a moderate to high risk that requires special controls. | 4 |