Duns Number:969752364
Device Description: DermaFlex Microcannula 30G/25mm + 27G/25mm Pilot
Catalog Number
DF30G25MM27G
Brand Name
Eclipse DermaFlex MicroCannula
Version/Model Number
DF30G25MM27G
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
K200017,K200017
Product Code
FMI
Product Code Name
Needle, Hypodermic, Single Lumen
Public Device Record Key
3d6059bd-e945-40df-a256-11310ebcf6e7
Public Version Date
March 31, 2021
Public Version Number
1
DI Record Publish Date
March 23, 2021
Package DI Number
10853602008526
Quantity per Package
25
Contains DI Package
00853602008529
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Box
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 14 |