Duns Number:649827193
Catalog Number
-
Brand Name
AutoLap Sterile Drape
Version/Model Number
ASS07022US
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
K131375,K152848,K131375,K152848
Product Code
GCJ
Product Code Name
Laparoscope, General & Plastic Surgery
Public Device Record Key
1d82ee74-c42d-4ac0-8581-457087624c91
Public Version Date
March 11, 2019
Public Version Number
4
DI Record Publish Date
February 13, 2017
Package DI Number
17290016648338
Quantity per Package
20
Contains DI Package
07290016648331
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
-
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 14 |