Duns Number:965399905
Device Description: The device is a sterile or sterilizable (via PVP-I or similar antiseptic) accessory intend The device is a sterile or sterilizable (via PVP-I or similar antiseptic) accessory intended to mark a set of locations on a patient's intact, uncompromised skin. The device is also intended to mark objects in the operational field of view. The device is intended to be used in clinical settings, by clinicians familiar with aseptic technique.
Catalog Number
-
Brand Name
Clear Guide VisiMARKER
Version/Model Number
CGVM
Device Commercial Distribution Status
In Commercial Distribution
Commercial Distribution End Date
-
Issuing Agency
In HIBCC
MRI safety Status
MR Safe
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
JAC
Product Code Name
System, X-Ray, Film Marking, Radiographic
Public Device Record Key
05984e54-aa8d-44d7-9917-16f29e88f934
Public Version Date
October 04, 2022
Public Version Number
3
DI Record Publish Date
September 21, 2016
Package DI Number
B201CGVM2
Quantity per Package
16
Contains DI Package
B201CGVM1
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. | 4 |