Primary Device ID | 10015127010006 |
NIH Device Record Key | cfd52d9d-35eb-441d-907c-7ef9837db0c2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Select Brand Tampons |
Version Model Number | SB22012F/1 |
Company DUNS | 012578514 |
Company Name | L. & R. DISTRIBUTORS, INC. |
Device Count | 20 |
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 | true |
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 | 00001512701003 [Unit of Use] |
GS1 | 00015127010009 [Primary] |
GS1 | 10015127010006 [Package] Contains: 00015127010009 Package: case [12 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 | 3 |
Public Version Date | 2020-01-20 |
Device Publish Date | 2016-11-10 |
10015127013533 | unscented cardboard applicator plus tampons |
10015127013526 | unscented cardboard applicator super tampons |
10015127013519 | unscented regular cardboard applicator tampons |
10015127010006 | unscented cardboard applicator super tampons |
20015127009991 | unscented cardboard applicator regular tampons |