Primary Device ID | 00814913024585 |
NIH Device Record Key | 1ff3227b-0929-42eb-ae3e-26fa2d657fe3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET II Fixture SA Regular No-Mounted |
Version Model Number | CET2R4008S |
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 | 00814913024585 [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 | 2017-11-17 |
00814913024776 | CET2R5015S |
00814913024769 | CET2R5013S |
00814913024752 | CET2R5011S |
00814913024745 | CET2R5010S |
00814913024738 | CET2R5008S |
00814913024721 | CET2R5007S |
00814913024714 | CET2R5006S |
00814913024691 | CET2R4515S |
00814913024684 | CET2R4513S |
00814913024677 | CET2R4511S |
00814913024660 | CET2R4510S |
00814913024653 | CET2R4508S |
00814913024646 | CET2R4507S |
00814913024639 | CET2R4018S |
00814913024622 | CET2R4015S |
00814913024615 | CET2R4013S |
00814913024608 | CET2R4011S |
00814913024592 | CET2R4010S |
00814913024585 | CET2R4008S |
00814913024578 | CET2R4007S |