Primary Device ID | 10850063931042 |
NIH Device Record Key | 04275469-9763-48c8-86d5-ef87acdd0ada |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Everylife Inc. |
Version Model Number | PD200 |
Company DUNS | 125725609 |
Company Name | EDEN FEMININE CARE LLC |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 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 | 10850063931042 [Primary] |
NUQ | Pad, Menstrual, Reusable |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-10 |
Device Publish Date | 2025-06-02 |
10850063931042 | cotton top sheet menstrual pad/regular absorbency |
00850063931144 | vaginal tampon with string and compact applicator | Super Plus absorbency |
00850063931137 | vaginal tampon with string and compact applicator | Super absorbency |
00850063931120 | vaginal tampon with string and compact applicator | Light absorbency |
00850063931106 | vaginal tampon with string and compact applicator | Mixed variety regular and super absorbency |