| Primary Device ID | 10070038203329 |
| NIH Device Record Key | ff4c71ec-33b8-4547-9a78-bfbd31105c30 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Best Choice Tampons |
| Version Model Number | BAWAS10 |
| Company DUNS | 868703513 |
| Company Name | VALU MERCHANDISERS COMPANY |
| Device Count | 10 |
| DM Exempt | false |
| Pre-market Exempt | false |
| 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 | true |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00070038203322 [Primary] |
| GS1 | 07290016625028 [Unit of Use] |
| GS1 | 10070038203329 [Package] Contains: 00070038203322 Package: CASE [24 Units] In Commercial Distribution |
| HEB | Tampon, Menstrual, Unscented |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2019-12-09 |
| Device Publish Date | 2016-09-20 |
| 10070038651403 | BAWUR18 |
| 10070038651397 | BAWUS18 |
| 10070038622663 | Multi pack of 36 - 8 light/20 Regular/8 Super |
| 10070038610639 | BAWGS18 |
| 10070038610615 | BAWGR20 |
| 10070038596025 | Multi pack of 40 - 8 light/16 Regular/16 Super |
| 10070038203329 | BAWAS10 |
| 10070038203312 | BAWAR10 |
| 10070038203305 | BAWAP40 |
| 10070038202728 | BAWAS40 |
| 10070038202711 | BAWAR40 |