| Primary Device ID | 00850047439147 |
| NIH Device Record Key | f0989321-4a2e-476c-b2c0-11010702c99a |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Mommy Matters |
| Version Model Number | MM-9000 |
| Company DUNS | 079956040 |
| Company Name | Joylux, 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 | true |
| 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 | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00850047439147 [Primary] |
| HGZ | Heater, Perineal, Direct Contact |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2025-03-12 |
| Device Publish Date | 2025-03-04 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() MOMMY MATTERS 88438444 not registered Live/Pending |
Mommy Matters 2019-05-20 |
![]() MOMMY MATTERS 88438418 not registered Live/Pending |
Mommy Matters 2019-05-20 |