| Primary Device ID | 07613327052404 |
| NIH Device Record Key | 1a70d07f-6922-4a34-8f5e-611f34081a11 |
| Commercial Distribution Discontinuation | 2018-12-07 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 0250080204 |
| Catalog Number | 0250-080-204 |
| Company DUNS | 187502109 |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| 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 | 07613327052404 [Primary] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327052404]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2018-12-07 |
| Device Publish Date | 2016-09-23 |
| 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 |
| 07613327262438 - XIA | 2025-09-11 AWL |