Primary Device ID | 08800121780889 |
NIH Device Record Key | 3e48a2b6-f594-4f36-a0e7-327926b96b9c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Estar-Z |
Version Model Number | ZP3A0014T |
Company DUNS | 694893867 |
Company Name | Osstem 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 | false |
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 | 08800121780889 [Primary] |
EIH | Powder, Porcelain |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-04 |
Device Publish Date | 2024-08-27 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ESTAR-Z 79308895 not registered Live/Pending |
OSSTEMIMPLANT CO., LTD. 2021-03-16 |