| Primary Device ID | 10078300029868 |
| NIH Device Record Key | 70059318-dc8a-46e4-9d97-d1d4fdc9e6a0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | OB |
| Version Model Number | 02986 |
| Company DUNS | 151179769 |
| Company Name | EDGEWELL PERSONAL CARE BRANDS, LLC |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 | 00078300029861 [Primary] |
| GS1 | 10078300029868 [Package] Contains: 00078300029861 Package: [12 Units] In Commercial Distribution |
| HEB | TAMPON, 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 | 2019-08-05 |
| Device Publish Date | 2019-07-26 |
| 10078300070211 | OB DIG PROC SUP BKA 40 |
| 10078300070204 | OB DIG PROC REG GK 40 |
| 20078300070157 | OB DIG PROC MP 40 |
| 10078300070143 | OB DIG PROC SUP BKA 18 |
| 10078300070136 | OB DIG PROC REG GK 18 |
| 10078300070129 | OB DIG HELIX ULTRA DK 40 |
| 20078300070119 | OB DIG HELIX MP 40 |
| 20078300070096 | OB DIG HELIX SUP BK 40 |
| 10078300070082 | OB DIG HELIX REG AL 40 |
| 20078300070102 | OB DIG HELIX SUP+ CK 40 |
| 10078300029936 | OB ORGANIC SUP APLC 18ct 4/3 |
| 10078300029868 | OB ORGANIC REG APLC 18ct 4/3 |
| 10078300029851 | OB ORGANIC SUP NO APLC 24ct 8/3 |
| 10078300029837 | OB ORGANIC REG NO APLC 24ct 8/3 |
| 10078300021794 | 40CT o.b. HELIX ULTRA 4/3 (US/CN) |