| 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 |