| Primary Device ID | 37613252518380 |
| NIH Device Record Key | 82965c46-6015-40a3-bc86-066e328bf1be |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 5450815107 |
| Catalog Number | 5450-815-107 |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 | 07613252518389 [Primary] |
| GS1 | 37613252518380 [Package] Contains: 07613252518389 Package: pack [5 Units] In Commercial Distribution |
| LFL | Instrument, ultrasonic surgical |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-10-25 |
| Device Publish Date | 2016-09-23 |
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