| Primary Device ID | 07613327651683 |
| NIH Device Record Key | b70c944c-9f49-40ac-8c98-1336ac56d48d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | mild Device Kit |
| Version Model Number | MDK-0001 |
| Catalog Number | MDK-0001 |
| Company DUNS | 011925561 |
| Company Name | VERTOS MEDICAL, INC. |
| 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 | true |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com | |
| Phone | 8779586227 |
| customerservice@vertosmed.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07613327651683 [Primary] |
| HIBCC | B235MDK00010 [Previous] |
| HRX | Arthroscope |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-12-02 |
| Device Publish Date | 2024-11-22 |
| B235MDK00010 | MDK-0001 |
| 07613327651683 | MDK-0001 |
| 07613327651676 | MDK-0002 |