Duns Number:825673239
Device Description: AMSafe® I.V. Administration Set75" (192cm) Long GRAVITY USE ONLY
Catalog Number
ABL006SIP-LND
Brand Name
AMSafe® I.V. Administration Set
Version/Model Number
1
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
-
Product Code
FPA
Product Code Name
Set, Administration, Intravascular
Public Device Record Key
89fa4d4c-ca05-4956-a24f-b1e4305416ae
Public Version Date
April 07, 2021
Public Version Number
4
DI Record Publish Date
September 18, 2017
Package DI Number
40704411006054
Quantity per Package
100
Contains DI Package
10704411006053
Package Discontinue Date
-
Package Status
In Commercial Distribution
Package Type
Case
| Device Class | Device Class Description | No of Devices |
|---|---|---|
| 1 | A medical device with low to moderate risk that requires general controls | 89 |
| 2 | A medical device with a moderate to high risk that requires special controls. | 411 |
| U | Unclassified | 1 |