| Primary Device ID | 37613327512367 |
| NIH Device Record Key | 504af3b7-e03e-4b42-a8fe-2a1eae15a83a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CrossBlade |
| Version Model Number | 0475337001 |
| Catalog Number | 0475-337-001 |
| Company DUNS | 187502109 |
| Company Name | STRYKER CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx | |
| Phone | +1(866)624-4422 |
| xx@xx.xx |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327512366 [Primary] |
| GS1 | 37613327512367 [Package] Contains: 07613327512366 Package: pack [5 Units] In Commercial Distribution |
| GFA | BLADE, SAW, GENERAL & PLASTIC SURGERY, SURGICAL |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2022-07-04 |
| Device Publish Date | 2020-11-09 |
| 37613327502740 | Bursector 4.0 mm x 125 mm. Do Not Resterilize, Do Not Use If Package Is Damaged, Keep Dry, Keep |
| 37613327502610 | Bursector 5.5 mm x 125 mm. Do Not Resterilize, Do Not Use If Package Is Damaged, Keep Dry, Keep |
| 37613327301541 | XL, Arthroscopic Shaver Blades, Diamond Round Bur. Do Not Resterilize, Do Not Use If Package Is |
| 37613327301534 | XL, Arthroscopic Shaver Blades, Diamond Round Bur. Do Not Resterilize, Do Not Use If Package Is |
| 37613327512343 | 0475361001 |
| 37613327512367 | 0475337001 |
| 37613327512350 | 0475341001 |
| 37613327512336 | 0475333001 |
| 37613327512329 | 0475345001 |
| 37613327512312 | 0475331001 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CROSSBLADE 85771325 4739474 Live/Registered |
Stryker Corporation 2012-11-05 |
![]() CROSSBLADE 85249127 not registered Dead/Abandoned |
JAKKS Pacific, Inc. 2011-02-23 |
![]() CROSSBLADE 77190801 3469035 Live/Registered |
TYR Sport, Inc. 2007-05-25 |