| Primary Device ID | 07613327004588 | 
| NIH Device Record Key | de03208c-a355-4055-834f-8749a808b777 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | TARGET XL | 
| Version Model Number | M0036116200 | 
| Catalog Number | 611620 | 
| Company DUNS | 042405446 | 
| Company Name | Stryker Corporation | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | false | 
| MRI Safety Status | MR Conditional | 
| 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 | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | |
| Phone | +1(855)916-3876 | 
| NVCustomerService@stryker.com | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Device Size Text, specify | 0 | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Special Storage Condition, Specify | Between 0 and 0 *Store in cool, dry, dark place. | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 07613327004588 [Primary] | 
| KRD | Device, Vascular, for Promoting Embolization | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 2 | 
| Public Version Date | 2018-03-29 | 
| Device Publish Date | 2015-09-21 | 
| 07613327128390 | 360 SOFT Detachable Coil | 
| 07613327128338 | 360 SOFT Detachable Coil | 
| 07613327128321 | 360 SOFT Detachable Coil | 
| 07613327128314 | 360 SOFT Detachable Coil | 
| 07613327128291 | 360 SOFT Detachable Coil | 
| 07613327128284 | 360 SOFT Detachable Coil | 
| 07613327128277 | 360 SOFT Detachable Coil | 
| 07613327128260 | 360 SOFT Detachable Coil | 
| 07613327004809 | Helical Detachable Coil | 
| 07613327004793 | 360 Standard Detachable Coil | 
| 07613327004786 | 360 Standard Detachable Coil | 
| 07613327004779 | 360 Standard Detachable Coil | 
| 07613327004762 | 360 Standard Detachable Coil | 
| 07613327004755 | 360 Standard Detachable Coil | 
| 07613327004748 | 360 Standard Detachable Coil | 
| 07613327004731 | 360 Standard Detachable Coil | 
| 07613327004724 | 360 Standard Detachable Coil | 
| 07613327004649 | 360 Soft Detachable Coil | 
| 07613327004632 | 360 Soft Detachable Coil | 
| 07613327004625 | 360 Soft Detachable Coil | 
| 07613327004618 | 360 Soft Detachable Coil | 
| 07613327004601 | 360 Soft Detachable Coil | 
| 07613327004595 | Helical Detachable Coil | 
| 07613327004588 | Helical Detachable Coil | 
| 07613327004571 | Helical Detachable Coil | 
| 07613327004564 | Helical Detachable Coil | 
| 07613327004557 | Helical Detachable Coil | 
| 07613327004540 | Helical Detachable Coil | 
| 07613327004533 | Helical Detachable Coil | 
| 04546540711618 | 360 Soft Detachable Coil | 
| 04546540711564 | 360 Soft Detachable Coil | 
| 04546540711557 | 360 Soft Detachable Coil | 
| 04546540711540 | 360 Soft Detachable Coil | 
| 04546540711533 | 360 Soft Detachable Coil | 
| 04546540711519 | Helical Detachable Coil | 
| 04546540711496 | Helical Detachable Coil | 
| 04546540711427 | Helical Detachable Coil | 
| 04546540711410 | Helical Detachable Coil | 
| 04546540711403 | Helical Detachable Coil | 
| 04546540711304 | 360 Standard Detachable Coil | 
| 04546540711298 | 360 Standard Detachable Coil | 
| 04546540711281 | 360 Standard Detachable Coil | 
| 04546540711274 | 360 Standard Detachable Coil | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() TARGET XL  88893496  not registered Live/Pending  | 
        Stryker Corporation  2020-04-29  | 
![]() TARGET XL  88893496  not registered Live/Pending  | 
        Stryker European Operations Limited  2020-04-29  | 
![]() TARGET XL  85724794  4426546 Live/Registered  | 
        Stryker NV Operations Limited  2012-09-10  | 
![]() TARGET XL  85724794  4426546 Live/Registered  | 
        Stryker Corporation  2012-09-10  |