| Primary Device ID | 07613154511501 |
| NIH Device Record Key | 93db6569-65ff-4c22-b2d6-f5a4f8faac60 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | CORE, Maestro |
| Version Model Number | 5400207000S1 |
| Catalog Number | 5400-207-000S1 |
| 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 | 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(800)253-3210 |
| Inst.Stryker.cs@Stryker.com |
| Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
| Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
| Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613154511501 [Primary] |
| HBB | MOTOR, DRILL, PNEUMATIC |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-07-05 |
| Device Publish Date | 2016-09-23 |
| 07613154511501 | Large Non-exhausting Footpedal |
| 07613154410224 | Universal Footpedal |
| 07613154284467 | Non-exhausting Footpedal |
| 04546540503947 | Drill with Handswitch |
| 04546540469144 | Footpedal |
| 04546540469113 | Drill |
| 34546540469107 | Diffuser |
| 34546540469091 | Oil Cartridge |