Primary Device ID | 00814913020723 |
NIH Device Record Key | 0841394a-f3e2-472b-be4b-fe78b2fad385 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET III Fixture SA Regular Pre-Mounted |
Version Model Number | AET3R4511S |
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 | 00814913020723 [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 | 2015-09-01 |
00814913020839 | AET3R5018S |
00814913020822 | AET3R5015S |
00814913020815 | AET3R5013S |
00814913020808 | AET3R5011S |
00814913020792 | AET3R5010S |
00814913020785 | AET3R5008S |
00814913020778 | AET3R5007S |
00814913020754 | AET3R4518S |
00814913020747 | AET3R4515S |
00814913020730 | AET3R4513S |
00814913020723 | AET3R4511S |
00814913020716 | AET3R4510S |
00814913020709 | AET3R4508S |
00814913020693 | AET3R4507S |
00814913020686 | AET3R4018S |
00814913020679 | AET3R4015S |
00814913020662 | AET3R4013S |
00814913020655 | AET3R4011S |
00814913020648 | AET3R4010S |
00814913020631 | AET3R4008S |
00814913020624 | AET3R4007S |