Duns Number:042928915
Device Description: 84” 10 drop, vented/non-vented drip chamber, roller clamp, pre-slit Y-site, needleless Y-s 84” 10 drop, vented/non-vented drip chamber, roller clamp, pre-slit Y-site, needleless Y-site connector,
Catalog Number
-
Brand Name
PMG0083
Version/Model Number
PMG0083
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
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
d5acc0ef-a8a9-4e5c-81fc-2b1bc6393d9d
Public Version Date
July 23, 2019
Public Version Number
1
DI Record Publish Date
July 15, 2019
Package DI Number
10850005864506
Quantity per Package
50
Contains DI Package
00850005864509
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. | 45 |