Primary Device ID | 00810125996108 |
NIH Device Record Key | f4f1ff15-3d3f-4ac1-ad6f-686a392b13aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET Convertible Abutment |
Version Model Number | ETCAS4020CP |
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 | 00810125996108 [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 | 2024-07-01 |
Device Publish Date | 2024-06-21 |
00810125996221 | ETCA6050CP |
00810125996214 | ETCA6040CP |
00810125996207 | ETCA6030CP |
00810125996191 | ETCA6020CP |
00810125996184 | ETCA6010CP |
00810125996177 | ETCA5050CP |
00810125996160 | ETCA5040CP |
00810125996153 | ETCA5030CP |
00810125996146 | ETCA5020CP |
00810125996139 | ETCA5010CP |
00810125996122 | ETCAS4040CP |
00810125996115 | ETCAS4030CP |
00810125996108 | ETCAS4020CP |
00810125996092 | ETCAS4010CP |
00810125996085 | ETCA4040CP |
00810125996078 | ETCA4030CP |
00810125996061 | ETCA4020CP |
00810125996054 | ETCA4010CP |