Primary Device ID | 10073010716923 |
NIH Device Record Key | 503e1716-3ea2-474c-8c51-2ab05c12177b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | L. |
Version Model Number | L. Tampon |
Company DUNS | 004238200 |
Company Name | PROCTER & GAMBLE MANUFACTURING COMPANY, THE |
Device Count | 60 |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00073010716926 [Primary] |
GS1 | 10073010716923 [Package] Contains: 00073010716926 Package: Case [240 Units] In Commercial Distribution |
GS1 | 40073010716924 [Package] Package: Pallet [1 Units] In Commercial Distribution |
GS1 | 50073010716921 [Unit of Use] |
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 | 2022-08-22 |
Device Publish Date | 2022-08-12 |
40073010717143 | L. Tampon Compact Regular |
10073010717128 | L. Tampon Full Size Regular |
10073010716923 | L. Tampon Full Size Regular |
20073010716562 | L. Tampon Full Size Mix - Regular, Super |
40073010716559 | L. Tampon Full Size Mix - Light, Regular |
10073010716541 | L. Tampon Full Size Super |
20073010716531 | L. Tampon Full Size Regular |
10073010716527 | L. Tampon Full Size Mix - Regular, Super |
20073010716517 | L. Tampon Full Size Mix - Light, Regular |
40073010716504 | L. Tampon Full Size Lightx |
10073010716206 | L. Tampon Full Size Mix - Regular, Super SIOC |
40073010718935 | L. Tampon Full Size Mix - Regular, Super SIOC |