DEVICE: GLIDECATH (04987350714886)
Device Identifier (DI) Information
GLIDECATH
CG431
In Commercial Distribution
RF*ZM74115JA
TERUMO CORPORATION
CG431
In Commercial Distribution
RF*ZM74115JA
TERUMO CORPORATION
RADIFOCUS GLIDECATH
Device Characteristics
Labeling does not contain MRI Safety Information | |
No | |
No | |
Yes | |
Yes | |
No | |
No | |
No | |
No |
GMDN
[?]GMDN© Term Code, Names and Definitions (*Terms of Use): GMDN® is a registered trademark of The GMDN Agency. All rights reserved. Used under licence from The GMDN Agency Ltd.
GMDN Term Code | GMDN Term Name | GMDN Term Definition | GMDN Term Status [?] | Implantable? |
---|---|---|---|---|
10688 | Angiographic catheter, single-use |
A thin, flexible tube designed to inject a contrast medium into select blood vessels of the cerebral, visceral, or peripheral vasculature during an angiographic procedure in order to facilitate the clear visualization of the vascular system of a targeted organ or area of the body. It is introduced percutaneously, has a radiopaque marker(s) for positioning, and may include disposable devices dedicated to catheter introduction/function [e.g., sheath(s)]. It may also be used for simultaneous pressure measurements to determine the transvalvular, intravascular, and intraventricular pressure gradients. This is a single-use device.
|
Active | false |
FDA Product Code
[?]Product Code | Product Code Name |
---|---|
DQO | CATHETER, INTRAVASCULAR, DIAGNOSTIC |
FDA Premarket Submission
FDA Premarket Submission Number [?] | Supplement Number [?] |
---|---|
Premarket Submission Number Not Available/Not Released |
Sterilization
Storage and Handling
[?]Storage and Handling |
---|
Special Storage Condition, Specify: Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10. |
Clinically Relevant Size
[?]Size Type Text |
---|
Length: 150 Centimeter |
Outer Diameter: 1.40 Millimeter |
Device Size Text, specify: Hydrophilic Coating Length : 40cm |
Device Size Text, specify: Max Guide Wire O.D. : .038" (0.97mm) |
Pressure: 5171 KiloPascal |
Device Record Status
79cd27eb-2ebb-4061-be46-7a4e13a97627
March 29, 2018
2
September 09, 2016
March 29, 2018
2
September 09, 2016
Alternative and Additional Identifiers Additional Identifiers
Package DI
[?]Package DI Number | Quantity per Package | Contains DI Package | Package Discontinue Date | Package Status | Package Type |
---|---|---|---|---|---|
34987350714887 | 5 | 04987350714886 | In Commercial Distribution | Shelfbox | |
54987350714881 | 5 | 34987350714887 | In Commercial Distribution | Carton |
Secondary DI
[?]Issuing Agency [?] | Secondary DI Number |
---|---|
No Secondary DIs found |
Unit of Use DI
[?]
Unit of Use DI Number:
No Unit of Use DI Numbers Found
CLOSE
Direct Marking (DM)
[?]Production Identifier(s) in UDI
[?]Customer Contact
[?]
+1(800)283-7866
tmccustomer.admin@terumomedical.com
tmccustomer.admin@terumomedical.com