Primary Device ID | 00810019240188 |
NIH Device Record Key | f228b7d8-d13a-4d72-92f4-13ab62365a10 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ET RIGID PROTECT CAP |
Version Model Number | ETRPC6004S |
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 | 00810019240188 [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 |
00810019240218 | ETRPC7005S |
00810019240201 | ETRPC6007S |
00810019240195 | ETRPC6005S |
00810019240188 | ETRPC6004S |
00810019240171 | ETRPC5007S |
00810019240164 | ETRPC5005S |
00810019240157 | ETRPC5004S |
00810019240140 | ETRPC4507 |
00810019240133 | ETRPC4505 |
00810019240126 | ETRPC4504 |
00810019240119 | ETRPC4007 |
00810019240102 | ETRPC4005 |
00810019240096 | ETRPC4004 |
00810125991066 | ETRPC670C |
00810125991073 | ETRPC760C |
00810125991059 | ETRPC660C |
00810125991035 | ETRPC570C |
00810125991028 | ETRPC560C |
00810125991011 | ETRPC540C |
00810125991004 | ETRPC471C |
00810125990991 | ETRPC461C |
00810125990977 | ETRPC470C |
00810125990960 | ETRPC460C |
00810125990953 | ETRPC440C |
00810125991042 | ETRPC640C |
00810125990984 | ETRPC441C |