Primary Device ID | 54987892058870 |
NIH Device Record Key | 7c879202-5151-4ed1-bad9-ba455cae87d0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FINECROSS |
Version Model Number | M3-1430 |
Catalog Number | NC*A853B |
Company DUNS | 690543319 |
Company Name | TERUMO CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 | true |
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)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com | |
Phone | +1(800)283-7866 |
tmccustomer.admin@terumomedical.com |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Length | 130 Centimeter |
Outer Diameter | 0.61 Millimeter |
Outer Diameter | 0.84 Millimeter |
Device Size Text, specify | 0 |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Special Storage Condition, Specify | Between 0 and 0 *Fragile. Keep dry. Keep away from sunlight. Stacking limit by 9. |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04987892058875 [Primary] |
GS1 | 54987892058870 [Package] Contains: 04987892058875 Package: Carton [5 Units] In Commercial Distribution |
DQY | Catheter, percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-06-28 |
Device Publish Date | 2022-06-20 |
54987350703182 | FINECROSS MG Coronary Micro-Guide Catheter |
54987350703168 | FINECROSS MG Coronary Micro-Guide Catheter |
54987892058870 | FineCross M3 Coronary Micro-Guide Catheter |
54987892058856 | FineCross M3 Coronary Micro-Guide Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FINECROSS 77223575 3581225 Live/Registered |
Terumo Kabushiki Kaisha 2007-07-06 |