Primary Device ID | 00763000659080 |
NIH Device Record Key | 5b4d3a1b-bf98-45b5-95a8-81641f53559d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlexCath Contour™ |
Version Model Number | 10FCC13 |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, INC. |
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 | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Length | 65.5 Centimeter |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Special Storage Condition, Specify | Between 0 and 0 *Keep Dry |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00763000659080 [Primary] |
DRA | CATHETER, STEERABLE |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-01-23 |
Device Publish Date | 2024-01-15 |
00763000659080 | SHEATH 10FCC13 FLEXCATH CONTOUR 10F US |
00763000659097 | SHEATH 10FCC20 FLEXCATH CONTOUR 10F US |
00763000234928 | SHEATH 12FCC13 FLEXCATH CONTOUR 12F US |
00763000234935 | SHEATH 12FCC20 FLEXCATH CONTOUR 12F US |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() FLEXCATH CONTOUR 97234659 not registered Live/Pending |
Medtronic CryoCath LP 2022-01-24 |
![]() FLEXCATH CONTOUR 88165303 not registered Live/Pending |
Medtronic CryoCath LP 2018-10-23 |