| Primary Device ID | 07613327052381 |
| NIH Device Record Key | a13edc4f-04d1-4131-9ac6-f3ee64914a5c |
| Commercial Distribution Discontinuation | 2019-01-11 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 0250080179 |
| Catalog Number | 0250-080-179 |
| 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 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327052381 [Primary] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327052381]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-01-11 |
| Device Publish Date | 2016-09-23 |
| 37613327548205 - Neptune SafeAir | 2025-01-14 Telescopic Smoke Evacuation Pencil, Push Button, Coated, No PVC |
| 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 |