Duns Number:118380146
Device Description: NanoClave™ Connector
Catalog Number
01C-A1000
Brand Name
ICU Medical
Version/Model Number
01C-A1000
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"
Yes
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
K970855,K970855
Product Code
FPA
Product Code Name
Set, administration, intravascular
Public Device Record Key
2e7506f4-b68c-45c7-95d7-0ff7e68f7b40
Public Version Date
November 03, 2021
Public Version Number
1
DI Record Publish Date
October 26, 2021
Package DI Number
10840619060371
Quantity per Package
100
Contains DI Package
00840619060374
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
CS
Device Class | Device Class Description | No of Devices |
---|---|---|
2 | A medical device with a moderate to high risk that requires special controls. | 4887 |