Primary Device ID | 00810126045003 |
NIH Device Record Key | ea44df9b-77ea-41cc-8e84-050289aa6df4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET III SA Ultra-Wide Fixture No Mount |
Version Model Number | CET3R6011S |
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 | 00810126045003 [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 | 2025-10-07 |
Device Publish Date | 2025-09-29 |
00814913024967 | CET3R7013S |
00814913024950 | CET3R7011S |
00814913024943 | CET3R7010S |
00814913024936 | CET3R7008S |
00814913024929 | CET3R7007S |
00814913024912 | CET3R7006S |
00814913024905 | AET3R6013S |
00814913024899 | CET3R6011S |
00814913024882 | CET3R6010S |
00814913024875 | CET3R6008S |
00814913024868 | CET3R6007S |
00814913024851 | CET3R6006S |
00810126045140 | CET3R7013S |
00810126045126 | CET3R7011S |
00810126045102 | CET3R7010S |
00810126045089 | CET3R7008S |
00810126045065 | CET3R7007S |
00810126045041 | CET3R7006S |
00810126045027 | CET3R6013S |
00810126045003 | CET3R6011S |
00810126044983 | CET3R6010S |
00810126044969 | CET3R6008S |
00810126044945 | CET3R6007S |
00810126044921 | CET3R6006S |