Primary Device ID | 00810125991233 |
NIH Device Record Key | 53f4f6ba-a317-4c19-8fb4-f8ecea3e8593 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET RIGID IMPRESSION COPING |
Version Model Number | ETRIC470SC |
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 | 00810125991233 [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 | 2024-07-11 |
Device Publish Date | 2024-07-03 |
00810019240478 | ETRIC7005S |
00810019240461 | ETRIC6007S |
00810019240454 | ETRIC6005S |
00810019240447 | ETRIC6004S |
00810019240430 | ETRIC5007S |
00810019240423 | ETRIC5005S |
00810019240416 | ETRIC5004S |
00810019240409 | ETRIC4507S |
00810019240393 | ETRIC4505S |
00810019240386 | ETRIC4504S |
00810019240379 | ETRIC4007S |
00810019240362 | ETRIC4005S |
00810019240355 | ETRIC4004S |
00810125991332 | ETRIC760SC |
00810125991325 | ETRIC670SC |
00810125991318 | ETRIC660SC |
00810125991301 | ETRIC640SC |
00810125991295 | ETRIC570SC |
00810125991288 | ETRIC560SC |
00810125991271 | ETRIC540SC |
00810125991264 | ETRIC471SC |
00810125991257 | ETRIC461SC |
00810125991240 | ETRIC441SC |
00810125991233 | ETRIC470SC |
00810125991226 | ETRIC460SC |
00810125991219 | ETRIC440SC |