ASAHI SION
GUDID 14547327082638
ASAHI INTECC CO., LTD.
Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use| Primary Device ID | 14547327082638 |
| NIH Device Record Key | e3e0eb47-4927-4049-98aa-f415ff109691 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ASAHI SION |
| Version Model Number | AHW14R301S |
| 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
| Length | 300 Centimeter |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
| Outer Diameter | 0.014 Inch |
| Length | 300 Centimeter |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04547327082631 [Primary] |
| GS1 | 14547327082638 [Package] Contains: 04547327082631 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 [ASAHI SION]
| 14547327086193 | AHW14R301J |
| 14547327086186 | AHW14R001J |
| 14547327082638 | AHW14R301S |
| 14547327082621 | AHW14R001S |
| 14547327133040 | AHW14R101J |
| 14547327132982 | AHW14R101S |
| 14547327132975 | AHW14R301P |
| 14547327132968 | AHW14R101P |
Trademark Results [ASAHI SION]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ASAHI SION 79113907 4232075 Dead/Cancelled |
ASAHI INTECC CO., LTD. 2012-02-21 |
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