Primary Device ID | 10834533001244 |
NIH Device Record Key | e4a07a38-377e-4aa8-b82f-e94112b673c5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Up&Up tampons |
Version Model Number | 245-04-0477 |
Company DUNS | 006961700 |
Company Name | TARGET CORPORATION |
Device Count | 18 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00834533001247 [Primary] |
GS1 | 07290016625110 [Unit of Use] |
GS1 | 10834533001244 [Package] Contains: 00834533001247 Package: CASE [6 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 | 2 |
Public Version Date | 2019-12-09 |
Device Publish Date | 2018-11-30 |
10834533004726 | 245-04-0408 |
10834533004542 | 245-04-0362 |
10834533004535 | 245-04-0370 |
10834533001244 | 245-04-0477 |
10834533001237 | 245-04-0501 |
10834533001206 | 245-04-0478 |
10834533001138 | Multi pack of 34 - 17 Regular/17 Super |
10834533000568 | 245-04-0058 |
10834533000490 | 245-04-0805 |
10834533000483 | 245-04-0806 |
10834533000315 | Up&Up Multi pack Tampons pack - 10 Light, 30 Regular and 10 Super Absorbency |
10834533004764 | 245-04-0521 |
10834533000285 | 245-04-0384 |
10834533000292 | 245-04-0387 |