Primary Device ID | 00821684073551 |
NIH Device Record Key | 21c77e26-320c-4615-a44a-bc79d200fbd4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HawkOneTM |
Version Model Number | H1-14550 |
Company DUNS | 968903703 |
Company Name | Covidien LP |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Storage Environment Temperature | Between -29 Degrees Fahrenheit and 140 Degrees Fahrenheit |
Storage Environment Temperature | Between -29 Degrees Fahrenheit and 140 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00821684073551 [Primary] |
MCW | Catheter, peripheral, atherectomy |
Steralize Prior To Use | true |
Device Is Sterile | true |
[00821684073551]
Radiation Sterilization
[00821684073551]
Radiation Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-08-26 |
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