| Primary Device ID | 07613327052329 |
| NIH Device Record Key | a0b0c3f2-7298-4104-9f8f-467be63b7571 |
| Commercial Distribution Discontinuation | 2020-02-03 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Version Model Number | 0250080156 |
| Catalog Number | 0250-080-156 |
| 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 | 07613327052329 [Primary] |
| GEI | ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[07613327052329]
Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2020-02-03 |
| Device Publish Date | 2016-09-23 |
| 07613327419252 - Patient Helper | 2024-12-23 |
| 37613327556651 - Neptune | 2024-12-23 SafeAir 125mm Suction Sleeve, Non-Sterile |
| 07613327643879 - Iconix | 2024-12-19 Iconix DC Guide for 2.3mm Anchor |
| 07613327643886 - Iconix | 2024-12-19 Iconix DC Obturator for 2.3 Anchor |
| 07613327644067 - Neptune | 2024-12-16 V2 SPECIMEN COLLECTION MANIFOLD |
| 07613327262469 - VBOSS | 2024-12-10 ENDPLATE TIP SMALL |
| 07613327262483 - VBOSS | 2024-12-10 ENDPLATE TIP LARGE |
| 07613327262506 - VBOSS | 2024-12-10 ENDPLATE TIP OFFSET |