Primary Device ID | B504OM588500350 |
NIH Device Record Key | 23e56b9e-5684-47cc-a65b-ed955efd1781 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Wright |
Version Model Number | 58850035 |
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 |
customersupport@provisiondrs.c | |
Phone | 541-480-7953 |
customersupport@provisiondrs.c |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B504OM588500350 [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 | 2019-02-25 |
Device Publish Date | 2019-01-24 |