Primary Device ID | 08809917603258 |
NIH Device Record Key | 605d48ea-b1bc-4cd3-9cbd-f21319f91f23 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Cover Screw |
Version Model Number | CS3402GR |
Company DUNS | 557821945 |
Company Name | ARUM DENTISTRY Co., Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 |
---|---|
GS1 | 08809917603258 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-13 |
Device Publish Date | 2024-05-03 |
08809917603265 | CS3403GR |
08809917603258 | CS3402GR |
08809917603241 | CS3401GR |
08809917603234 | CS3400GR |
08809917603227 | CS2803GM |
08809917603210 | CS2802GM |
08809917603203 | CS2801GM |
08809917603197 | CS2800GM |
08809917603180 | CS3403R |
08809917603173 | CS3402R |
08809917603166 | CS3401R |
08809917603159 | CS3400R |
08809917603142 | CS2803M |
08809917603135 | CS2802M |
08809917603128 | CS2801M |