Primary Device ID | 00810019248887 |
NIH Device Record Key | 72b43692-f7be-48d9-943d-4489b961c561 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EK Freeform ST Abutment Straight 5.0(1.5), Non-hex |
Version Model Number | EKFAS5015NTH |
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 | false |
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 | 00810019248887 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-05-31 |
Device Publish Date | 2022-05-23 |
00810125999703 - ET Stud abutment | 2024-12-31 |
00810125999710 - ET STUD ABUTMENT | 2024-12-31 |
00810125999727 - ET STUD ABUTMENT | 2024-12-31 |
00810125999734 - ET STUD ABUTMENT | 2024-12-31 |
00810125999741 - ET STUD ABUTMENT | 2024-12-31 |
00810125999758 - ET STUD ABUTMENT | 2024-12-31 |
00810125999765 - ET STUD ABUTMENT | 2024-12-31 |
00810125999772 - ET STUD ABUTMENT | 2024-12-31 |