Duns Number:315018218
Device Description: PRIMELINE PRO Lid (Outer), Standard 1/2, aluminium anodized, red, outer length: 303 mm, ou PRIMELINE PRO Lid (Outer), Standard 1/2, aluminium anodized, red, outer length: 303 mm, outer width: 294 mm, outer heigth: 37 mm
Catalog Number
JP121
Brand Name
PRIMELINE PRO
Version/Model Number
JP121
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
-
Prescription Use (Rx)
-
Over the Counter (OTC)
Yes
Kit
-
Combination Product
-
Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)
-
FDA Premarket Submission
-
Product Code
KCT
Product Code Name
Sterilization wrap containers, trays, cassettes & other accessories
Public Device Record Key
c3616b1e-2e83-4dfc-9010-8657beee5e0d
Public Version Date
July 08, 2021
Public Version Number
3
DI Record Publish Date
May 21, 2018
Package DI Number
None
Quantity per Package
-
Contains DI Package
-
Package Discontinue Date
-
Package Status
-
Package Type
-
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 11840 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 7088 |
| 3 | A medical device with high risk that requires premarket approval | 37 |