EXTENSION
GUDID 14547327076934
ASAHI INTECC CO., LTD.
Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension Coronary artery guidewire extension| Primary Device ID | 14547327076934 |
| NIH Device Record Key | 5220082d-8d34-444a-ad67-f800696257b9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | EXTENSION |
| Version Model Number | AG149000 |
| Company DUNS | 690711189 |
| Company Name | ASAHI INTECC CO., LTD. |
| 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 | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Device Dimensions
| Outer Diameter | 0.014 Inch |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 150 Centimeter |
| Outer Diameter | 0.014 Inch |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04547327076937 [Primary] |
| GS1 | 14547327076934 [Package] Contains: 04547327076937 Package: [5 Units] In Commercial Distribution |
FDA Product Code
| DQX | WIRE, GUIDE, CATHETER |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | true |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-11-22 |
| Device Publish Date | 2016-09-16 |
On-Brand Devices [EXTENSION]
| 14547327076934 | AG149000 |
| 14547327083574 | AG149001 |
Trademark Results [EXTENSION]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 EXTENSION 88416523 5948241 Live/Registered |
eXtension Foundation 2019-05-06 |
 EXTENSION 79139083 4508754 Live/Registered |
ASAHI INTECC CO., LTD. 2013-08-26 |
 EXTENSION 77120985 3458954 Dead/Cancelled |
triPRACTIX, LLC 2007-03-02 |
 EXTENSION 77051734 3373595 Live/Registered |
eXtension Foundation 2006-11-28 |
 EXTENSION 77051180 3392484 Dead/Cancelled |
eXtension Foundation 2006-11-27 |
 EXTENSION 76154994 not registered Dead/Abandoned |
Propaganda Films, Inc. 2000-10-26 |
 EXTENSION 76154983 not registered Dead/Abandoned |
Propaganda Films, Inc. 2000-10-26 |
 EXTENSION 74091478 1688281 Dead/Cancelled |
Noxell Corporation 1990-08-23 |
 EXTENSION 73503040 1406148 Dead/Cancelled |
EXECUTONE INC. 1984-10-09 |
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