Primary Device ID | 38016867007222 |
NIH Device Record Key | 73536202-e661-41b2-ad73-cfe9b7f2d98e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EARTH FARE |
Version Model Number | No Applicator Super |
Company DUNS | 428129167 |
Company Name | CORMAN SPA |
Device Count | 20 |
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 | false |
Manufacturing Date | false |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08016867007221 [Primary] |
GS1 | 18016867007228 [Unit of Use] |
GS1 | 38016867007222 [Package] Contains: 08016867007221 Package: [12 Units] In Commercial Distribution |
HEB | Tampon, Menstrual, Unscented |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-06-10 |
Device Publish Date | 2017-02-23 |
38016867007246 | Applicator Super |
38016867007239 | Applicator Regular |
38016867007222 | No Applicator Super |
08016867007214 | No Applicator Regular |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() EARTH FARE 88045079 5690844 Live/Registered |
Earth Fare, Inc. 2018-07-19 |
![]() EARTH FARE 78750308 3148741 Live/Registered |
Earth Fare, Inc. 2005-11-09 |
![]() EARTH FARE 77118739 not registered Dead/Abandoned |
Earth Fare, Inc. 2007-02-28 |
![]() EARTH FARE 75711881 2460264 Live/Registered |
Earth Fare, Inc. 1999-05-21 |
![]() EARTH FARE 75204303 2160095 Live/Registered |
EARTH FARE, INC. 1996-11-26 |