Primary Device ID | 00814913023465 |
NIH Device Record Key | 9ced7480-471a-42cb-93a9-d14c68ed7d5b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET Healing Abutment |
Version Model Number | ETHLA7005R |
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 | 00814913023465 [Primary] |
NHA | Abutment, Implant, Dental, Endosseous |
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 | 2015-09-08 |
00814913023472 | ETHLA7007R |
00814913023465 | ETHLA7005R |
00814913023458 | ETHLA7004R |
00814913023441 | ETHLA7003R |
00814913023434 | ETHLA6007R |
00814913023427 | ETHLA6005R |
00814913023410 | ETHLA6004R |
00814913023403 | ETHLA6003R |
00814913023397 | ETHLA5007R |
00814913023380 | ETHLA5005R |
00814913023373 | ETHLA5004R |
00814913023366 | ETHLA5003R |
00814913023359 | ETHLA4507R |
00814913023342 | ETHLA4507M |
00814913023335 | ETHLA4505R |
00814913023328 | ETHLA4505M |
00814913023311 | ETHLA4504R |
00814913023304 | ETHLA4504M |
00814913023298 | ETHLA4503R |
00814913023281 | ETHLA4503M |
00814913023274 | ETHLA4007R |
00814913023267 | ETHLA4007M |
00814913023250 | ETHLA4005R |
00814913023243 | ETHLA4005M |
00814913023236 | ETHLA4004R |
00814913023229 | ETHLA4004M |
00814913023212 | ETHLA4003R |
00814913023205 | ETHLA4003M |