Primary Device ID | 08806388229741 |
NIH Device Record Key | 4b83cee1-5a1d-407f-a2a2-c79c790cba02 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Multi-unit Abutment Screw |
Version Model Number | MUS35 |
Catalog Number | MUS35 |
Company DUNS | 687388178 |
Company Name | Megagen Implant Co. Ltd |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
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 | true |
Manufacturing Date | true |
Expiration Date | false |
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 | 08806388229741 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | true |
Device Is Sterile | false |
[08806388229741]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2015-06-23 |
08806388229765 | AnyOne Internal M2/ C=5.5 |
08806388229758 | AnyOne Internal M2/ C=4.5 |
08806388229741 | AnyOne Internal M2/ C=3.5 |
08806388229734 | AnyOne Internal M2/ C=2.5 |
08806388229727 | AnyOne Internal M2/ C=1.5 |
08806388243983 | M1.8 |
08806388243976 | M1.8 |
08806388243969 | M2/ L=6.8 |
08806388243952 | M2/ L=6.8 |
08806388243945 | C=5/ M2 |
08806388243938 | C=4/ M2 |
08806388243921 | C=3/ M2 |
08806388243914 | C=2/ M2 |
08806388243907 | C=1/ M2 |
08809708751199 | MUAAROS |