| Primary Device ID | 37613327117050 |
| NIH Device Record Key | e33c08a0-4727-4272-9569-fa6956a5b4d5 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5100901908 |
| Catalog Number | 5100-901-908 |
| 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 | false |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327117059 [Primary] |
| GS1 | 37613327117050 [Package] Contains: 07613327117059 Package: pack [2 Units] In Commercial Distribution |
| EIA | UNIT, OPERATIVE DENTAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 8 |
| Public Version Date | 2020-01-20 |
| Device Publish Date | 2016-09-23 |
| 07613327266849 - MANTIS | 2024-08-01 MANTIS POLY ADJUSTMENT DRIVER |
| 07613327582949 - Surpass Elite | 2024-07-29 Flow Diverter System |
| 07613327582994 - Surpass Elite | 2024-07-29 Flow Diverter System |
| 07613327583021 - Surpass Elite | 2024-07-29 Flow Diverter System |
| 07613327583106 - Surpass Elite | 2024-07-29 Flow Diverter System |
| 07613327583113 - Surpass Elite | 2024-07-29 Flow Diverter System |
| 07613327583120 - Surpass Elite | 2024-07-29 Flow Diverter System |
| 07613327583137 - Surpass Elite | 2024-07-29 Flow Diverter System |