Primary Device ID | B504OM8020750 |
NIH Device Record Key | c9c5a6a7-171c-4de8-826b-317df152d04c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Acumed |
Version Model Number | 80-2075 |
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 |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B504OM8020750 [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 | 2021-06-14 |
Device Publish Date | 2021-06-04 |
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 |