Duns Number:071595540
Device Description: 3mm Introducer with Sterile Single-Use Insufflation Needle
Catalog Number
MK-3500
Brand Name
MICROLAP
Version/Model Number
MK-3500
Device Commercial Distribution Status
Not in Commercial Distribution
Commercial Distribution End Date
December 08, 2020
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
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
HET
Product Code Name
LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
Public Device Record Key
9375346c-66ae-4c6e-8ac7-5ea4d087cfd0
Public Version Date
December 08, 2020
Public Version Number
3
DI Record Publish Date
September 24, 2016
Package DI Number
20653405037511
Quantity per Package
10
Contains DI Package
30653405037518
Package Discontinue Date
December 08, 2020
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 |