| Primary Device ID | 04546540132482 |
| NIH Device Record Key | 024f0343-547f-4a7f-8eaf-b08e30cde98a |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0986500000 |
| Catalog Number | 0986500000 |
| Company DUNS | 196548481 |
| 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 | 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 | 04546540132482 [Primary] |
| LGH | INSTRUMENT, CAST REMOVAL, AC-POWERED |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-25 |
| Device Publish Date | 2018-09-24 |
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