| Primary Device ID | 07613327051629 |
| NIH Device Record Key | 546777a6-9b63-4de5-90b8-8f8707a46c3e |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0233050084 |
| Catalog Number | 0233-050-084 |
| Company DUNS | 187502109 |
| 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 | true |
| 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(866)624-4422 |
| xx@xx.xx |
| Length | 10 Feet |
| Lumen/Inner Diameter | 5 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327051629 [Primary] |
| FCW | Light source, fiberoptic, routine |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327051629]
Ethylene Oxide;Moist Heat or Steam Sterilization;Hydrogen Peroxide
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-23 |
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