Primary Device ID | 08800039380638 |
NIH Device Record Key | b39653f4-4348-40c0-a23c-1c0d044b3d48 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Magic FC |
Version Model Number | IBS4507FC |
Company DUNS | 631169224 |
Company Name | InnoBioSurg Co.,Ltd(IBS implant Co.,Ltd) |
Device Count | 1 |
DM Exempt | true |
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 | 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 | 08800039380638 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-08-25 |
Device Publish Date | 2020-08-17 |
08800039380591 | IBS4007FC |
08800039380829 | IBS6513FC |
08800039380812 | IBS6511FC |
08800039380805 | IBS6509FC |
08800039380782 | IBS6013FC |
08800039380775 | IBS6011FC |
08800039380768 | IBS6009FC |
08800039380751 | IBS6007FC |
08800039380744 | IBS5513FC |
08800039380737 | IBS5511FC |
08800039380720 | IBS5509FC |
08800039380713 | IBS5507FC |
08800039380706 | IBS5013FC |
08800039380690 | IBS5011FC |
08800039380683 | IBS5009FC |
08800039380676 | IBS5007FC |
08800039380669 | IBS4513FC |
08800039380652 | IBS4511FC |
08800039380645 | IBS4509FC |
08800039380638 | IBS4507FC |
08800039380621 | IBS4013FC |
08800039380614 | IBS4011FC |
08800039380607 | IBS4009FC |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MAGIC FC 88141560 not registered Live/Pending |
Spartan FC 2018-10-03 |