| Primary Device ID | 07613327051636 |
| NIH Device Record Key | cb1287e6-610e-405d-98e2-efbcdc45e138 |
| Commercial Distribution Status | In Commercial Distribution |
| Version Model Number | 0233050090 |
| Catalog Number | 0233-050-090 |
| 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 | 07613327051636 [Primary] |
| FCW | Light source, fiberoptic, routine |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327051636]
Moist Heat or Steam Sterilization;Ethylene Oxide;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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| 07613327273120 - TRIO | 2025-01-03 PEDICULAR SCREWDRIVER SHAFT |
| 07613327273144 - TRIO + | 2025-01-03 SELF HOLDING PEDICULAR SCREWDRIVER |
| 07613327273175 - TRIO + | 2025-01-03 FLEXIBLE EXTENDER III |
| 07613327273182 - TRIO | 2025-01-03 ROD BENDER |
| 07613327273205 - TRIO | 2025-01-03 SPONDYLOSISTHESIS REDUCTION INSTRUMENT |
| 07613327273212 - TRIO | 2025-01-03 SPONDYLOLISTHESIS REDUCTION INSTRUMENT |
| 07613327273243 - TRIO + | 2025-01-03 FLEXIBLE EXTENDER II |