Primary Device ID | 00814913020525 |
NIH Device Record Key | ee2926b0-6171-478c-96d6-7220c26c6b4c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HIOSSEN |
Version Model Number | AET3M3010S |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00814913020525 [Primary] |
DZE | Implant, Endosseous, Root-Form |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-21 |
00814913020556 | AET3M3015S |
00814913020549 | AET3M3013S |
00814913020532 | AET3M3011S |
00814913020525 | AET3M3010S |
00814913020518 | AET3M3008S |
00814913020006 | AET3M3508B |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() HIOSSEN 77264620 3547792 Live/Registered |
OSSTEM IMPLANT, CO., LTD. 2007-08-27 |