| Primary Device ID | 37613327376341 |
| NIH Device Record Key | 244d6e2d-01b0-4025-b11e-65d19fd34ff1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | PostFree |
| Version Model Number | 3105000801 |
| Catalog Number | 3105-000-801 |
| 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 | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327376340 [Primary] |
| GS1 | 37613327376341 [Package] Contains: 07613327376340 Package: pack [1 Units] In Commercial Distribution |
| HST | Apparatus, traction, non-powered |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-08-31 |
| 07613327272246 - ARIA | 2025-09-25 IMPLANT IMPACTOR |
| 37613327405317 - SurgiCount Safety-Sponge | 2025-09-16 Laparotomy Sponge |
| 07613327262209 - XIA | 2025-09-11 FRENCH BENDER |
| 07613327262216 - XIA | 2025-09-11 SPREADER |
| 07613327262254 - XIA | 2025-09-11 COMPRESSOR |
| 07613327262261 - XIA | 2025-09-11 BLUNT PROBE |
| 07613327262292 - XIA | 2025-09-11 TORQUE WRENCH |
| 07613327262414 - XIA | 2025-09-11 STANDARD T-HANDLE |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() POSTFREE 87845637 not registered Live/Pending |
Stryker Corporation 2018-03-22 |