| Primary Device ID | 04546540688767 |
| NIH Device Record Key | 2e038123-f428-4ae5-bf68-4189492955a7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | SYNCHRO 2 |
| Version Model Number | M00326410 |
| Catalog Number | 2641 |
| Company DUNS | 042405446 |
| Company Name | Stryker Corporation |
| 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 |
| Phone | +1(855)916-3876 |
| NVCustomerService@stryker.com |
| Length | 200 Centimeter |
| Outer Diameter | 0.014 Inch |
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04546540688767 [Primary] |
| DQX | WIRE, GUIDE, CATHETER |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-21 |
| 04546540688798 | Standard Pre-shaped Guidewire with Hydrophilic Coating |
| 04546540688781 | Standard Guidewire with Hydrophilic Coating |
| 04546540688774 | Standard Pre-shaped Guidewire with Hydrophilic Coating |
| 04546540688767 | Standard Guidewire with Hydrophilic Coating |
| 04546540688750 | Soft Pre-shaped Guidewire with Hydrophilic Coating |
| 04546540688743 | Soft Guidewire with Hydrophilic Coating |
| 04546540688736 | Soft Pre-shaped Guidewire with Hydrophilic Coating |
| 04546540688729 | Soft Guidewire with Hydrophilic Coating |