Primary Device ID | 00810019245596 |
NIH Device Record Key | a5d47dc3-d742-41e9-9ce5-5ea5c4b17f26 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EK Healing Abutment |
Version Model Number | EKHA605 |
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 | 00810019245596 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-02-22 |
Device Publish Date | 2022-02-14 |
00810019245695 | EKHA805 |
00810019245688 | EKHA709 |
00810019245671 | EKHA707 |
00810019245664 | EKHA706 |
00810019245657 | EKHA705 |
00810019245640 | EKHA704 |
00810019245633 | EKHA703 |
00810019245626 | EKHA609 |
00810019245619 | EKHA607 |
00810019245602 | EKHA606 |
00810019245596 | EKHA605 |
00810019245589 | EKHA604 |
00810019245572 | EKHA603 |
00810019245565 | EKHA509 |
00810019245558 | EKHA507 |
00810019245541 | EKHA506 |
00810019245534 | EKHA505 |
00810019245527 | EKHA504 |
00810019245510 | EKHA503 |
00810019245503 | EKHA459 |
00810019245497 | EKHA457 |
00810019245480 | EKHA456 |
00810019245473 | EKHA455 |
00810019245466 | EKHA454 |
00810019245459 | EKHA453 |
00810019245442 | EKHA409 |
00810019245435 | EKHA407 |
00810019245428 | EKHA406 |
00810019245411 | EKHA405 |
00810019245404 | EKHA404 |
00810019245398 | EKHA403 |