| Primary Device ID | 07613327052398 |
| NIH Device Record Key | efac68d5-6e70-4936-975f-d78c355e321c |
| Commercial Distribution Discontinuation | 2020-03-26 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 0250080180 |
| Catalog Number | 0250-080-180 |
| 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 | 07613327052398 [Primary] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327052398]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 6 |
| Public Version Date | 2020-03-26 |
| Device Publish Date | 2016-09-23 |
| 07613327623338 - AXS Lift | 2025-03-12 Intracranial Base Catheter |
| 07613327623352 - AXS Lift | 2025-03-12 Intracranial Base Catheter |
| 07613327623376 - AXS Lift | 2025-03-12 Intracranial Base Catheter |
| 07613327623390 - AXS Lift | 2025-03-12 Intracranial Base Catheter |
| 07613327006094 - ARIA | 2025-03-10 ANCHORING PIN DRIVER |
| 07613327262865 - XIA | 2025-03-10 FORCEPS FOR MAC CONNECTOR |
| 07613327262889 - XIA II | 2025-03-10 ROD ROTATION FORCEPS |
| 07613327263169 - XIA II | 2025-03-10 POLYAXIAL SCREWDRIVER, XIA 3 STYLE |