Primary Device ID | 00810019241628 |
NIH Device Record Key | 4f06473d-46a6-404a-aa58-9d7734b9e1e6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET BITE INDEX |
Version Model Number | ETBIS5504S |
Company DUNS | 796083090 |
Company Name | HIOSSEN, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 00810019241628 [Primary] |
NDP | Accessories, 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 | 2019-05-23 |
Device Publish Date | 2019-05-15 |
00810019241666 | ETBIS5512S |
00810019241659 | ETBIS5510S |
00810019241642 | ETBIS5508S |
00810019241635 | ETBIS5506S |
00810019241628 | ETBIS5504S |
00810019241611 | ETBIM4512S |
00810019241604 | ETBIM4510S |
00810019241598 | ETBIM4508S |
00810019241581 | ETBIM4506S |
00810019241574 | ETBIM4504S |
00810125994630 | ETBIS5512SC |
00810125994623 | ETBIS5510SC |
00810125994616 | ETBIS5508SC |
00810125994609 | ETBIS5506SC |
00810125994593 | ETBIS5504SC |
00810125994586 | ETBIM4512SC |
00810125994579 | ETBIM4510SC |
00810125994562 | ETBIM4508SC |
00810125994555 | ETBIM4506SC |
00810125994548 | ETBIM4504SC |