| Primary Device ID | 34546540865053 |
| NIH Device Record Key | d853abd1-0c3d-46b9-bb9c-25543e22552d |
| Commercial Distribution Discontinuation | 2019-03-31 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 0215089000 |
| Catalog Number | 0215-089-000 |
| 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 | 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 | 04546540865052 [Primary] |
| GS1 | 34546540865053 [Package] Contains: 04546540865052 Package: pack [10 Units] Discontinued: 2019-03-31 Not in Commercial Distribution |
| GCY | APPARATUS, SUCTION, SINGLE PATIENT USE, PORTABLE, NONPOWERED |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2020-02-19 |
| Device Publish Date | 2018-09-24 |
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