| Primary Device ID | 37613154680840 |
| NIH Device Record Key | 9bcbd99b-00d1-42fd-aa31-c8d92a2f2672 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0702040000 |
| Catalog Number | 0702040000 |
| Company DUNS | 196548481 |
| 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(800)253-3210 |
| Inst.Stryker.cs@Stryker.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613154680849 [Primary] |
| GS1 | 37613154680840 [Package] Contains: 07613154680849 Package: pack [4 Units] In Commercial Distribution |
| JCX | APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2020-01-20 |
| Device Publish Date | 2016-09-23 |
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| 37613327405287 - SurgiCount Safety-Sponge | 2025-09-04 OR Towel |
| 37613327405294 - SurgiCount Safety-Sponge | 2025-09-04 Gauze Sponge |
| 37613327405300 - SurgiCount Safety-Sponge | 2025-09-04 Gauze Sponge |
| 37613327405324 - SurgiCount Safety-Sponge | 2025-09-04 Gauze Sponge |
| 37613327405331 - SurgiCount Safety-Sponge | 2025-09-04 OR Towel |
| 37613327405348 - SurgiCount Safety-Sponge | 2025-09-04 Laparotomy Sponge |
| 37613327405355 - SurgiCount Safety-Sponge | 2025-09-04 OR Towel |