Primary Device ID | 00847536041783 |
NIH Device Record Key | ae352b82-51f9-411e-8bde-4055b5294266 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PhenomTM 17 Catheter |
Version Model Number | FG11160-0615-2X |
Company DUNS | 826110710 |
Company Name | Micro Therapeutics, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight Keep Dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00847536041783 [Primary] |
KRA | Catheter, continuous flush |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-30 |
Device Publish Date | 2019-04-22 |
00847536041783 | CATHETER FG11160-0615-2X V04 |
00847536041776 | CATHETER FG11160-0615-2S V04 |
00847536041769 | CATHETER FG11160-0615-2R V04 |
00847536041752 | CATHETER FG11160-0615-2J V04 |
00847536041745 | CATHETER FG11160-0615-1S V04 |
00847536041738 | CATHETER FG11150-0615-2X V04 |
00847536041721 | CATHETER FG11150-0615-2S V04 |
00847536041714 | CATHETER FG11150-0615-2R V04 |
00847536041707 | CATHETER FG11150-0615-2J V04 |
00763000399672 | CATHETER FG11150-0615-2X V06 US |
00763000399665 | CATHETER FG11150-0615-2S V06 US |
00763000399658 | CATHETER FG11150-0615-2R V06 US |
00763000399641 | CATHETER FG11150-0615-2J V06 US |