Duns Number:071595540
Device Description: HYFRE-VAC II SMOKE EVACUATION SYSTEM, HAND HELD TUBING SET
Catalog Number
7-900-13
Brand Name
HYFRE-VAC II
Version/Model Number
7-900-13
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"
-
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
FYD
Product Code Name
APPARATUS, EXHAUST, SURGICAL
Public Device Record Key
f3231b58-829c-47d6-8350-0bc2c42aee35
Public Version Date
October 21, 2019
Public Version Number
5
DI Record Publish Date
September 24, 2016
Package DI Number
20653405043529
Quantity per Package
5
Contains DI Package
30653405043526
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CARTON
| 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 |