| Primary Device ID | 00990498500260 |
| NIH Device Record Key | ddf98f17-b9e9-4c4a-882d-1983cbc23a99 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Iris + Arlo |
| Version Model Number | 1 |
| Company DUNS | 144884489 |
| Company Name | Iris + Arlo 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 | 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 | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00990498500260 [Primary] |
| HHD | Pad, Menstrual, Unscented |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-01-14 |
| Device Publish Date | 2026-01-06 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IRIS + ARLO 79386807 not registered Live/Pending |
9459-8430 QUÃBEC INC. 2023-08-21 |