Primary Device ID | 00889024015678 |
NIH Device Record Key | 08b4e637-5903-4aed-8426-61788ab02d4d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Driva® |
Version Model Number | OP2.3D |
Company DUNS | 103167086 |
Company Name | ZIMMER DENTAL INC. |
Device Count | 1 |
DM Exempt | false |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00889024015678 [Primary] |
DZA | Drill, Dental, Intraoral |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-01-09 |
Device Publish Date | 2017-08-18 |
00889024015708 | OP4.2D |
00889024015692 | OP3.5D |
00889024015685 | OP2.8D |
00889024015678 | OP2.3D |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
DRIVA 97714806 not registered Live/Pending |
DRIVA SA 2022-12-13 |
DRIVA 79180512 5088897 Live/Registered |
Driva SA 2015-10-29 |