FIELDER
GUDID 14547327062784
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 | 14547327062784 |
| NIH Device Record Key | 4371d671-3bd6-47d4-8ef5-8abe5b1c9820 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FIELDER |
| Version Model Number | AGP140300J |
| 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 | 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04547327062787 [Primary] |
| GS1 | 14547327062784 [Package] Contains: 04547327062787 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 [FIELDER]
| 14547327062784 | AGP140300J |
| 14547327062777 | AGP140000J |
| 14547327056691 | AGP140300 |
| 14547327056684 | AGP140000 |
Trademark Results [FIELDER]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FIELDER 97358708 not registered Live/Pending |
Adam Fielder & Associates, LLC 2022-04-12 |
FIELDER 97358708 not registered Live/Pending |
Fielder Tree Service, LLC 2022-04-12 |
 FIELDER 77042826 3415119 Live/Registered |
ASAHI INTECC CO., LTD. 2006-11-13 |
 FIELDER 75977218 2170472 Dead/Cancelled |
Del Monte Fresh Produce N.A., Inc. 1993-12-17 |
 FIELDER 74802535 1951623 Dead/Cancelled |
Del Monte Fresh Produce N.A., Inc. 1993-12-17 |
 FIELDER 74470589 not registered Dead/Abandoned |
Del Monte Fresh Produce N.A., Inc. 1993-12-17 |
 FIELDER 74470588 1952235 Dead/Cancelled |
Del Monte Fresh Produce N.A., Inc. 1993-12-17 |
 FIELDER 73110920 1073562 Dead/Cancelled |
Sears, Roebuck and Co. 1976-12-27 |
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