| Primary Device ID | B504OMAT2M18130 |
| NIH Device Record Key | b4b37115-2dd6-4927-8173-2074d89fa59b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Acumed |
| Version Model Number | AT2M-1813 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| 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 | true |
| 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 | 541-480-7953 |
| mark@provisiondrs.com | |
| Phone | 541-480-7953 |
| mark@provisiondrs.com |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504OMAT2M18130 [Primary] |
| HTW | Bit, Drill |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-24 |
| Device Publish Date | 2018-08-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACUMED 88335799 not registered Live/Pending |
AcuMed Unlimited Inc 2019-03-12 |
![]() ACUMED 86326674 4682006 Live/Registered |
Acumed, LLC 2014-07-02 |
![]() ACUMED 85563896 4225361 Live/Registered |
Acumed LLC 2012-03-08 |
![]() ACUMED 85447950 4224449 Dead/Cancelled |
Knowledgepoint360 Group LLC 2011-10-14 |
![]() ACUMED 74545470 1931036 Live/Registered |
ACUMED LLC 1994-07-05 |
![]() ACUMED 73688989 not registered Dead/Abandoned |
RICHARDSON-VICKS INC. 1987-10-13 |