Primary Device ID | 06430060159983 |
NIH Device Record Key | 35283268-1a97-48e7-b207-a406da171268 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Fertile Window |
Version Model Number | Fertile Window Android |
Company DUNS | 081094249 |
Company Name | Ouraring Inc. |
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 | false |
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 | 06430060159983 [Primary] |
LHD | Device, Fertility Diagnostic, Proceptive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-11-20 |
Device Publish Date | 2024-11-12 |
06430060159990 | Fertile Window iOS |
06430060159983 | Fertile Window Android |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
FERTILE WINDOW 75593980 not registered Dead/Abandoned |
Conception Technology Incorporated 1998-11-23 |