Primary Device ID | 10194346231437 |
NIH Device Record Key | 67c1e836-b90d-42e1-835b-75bfcecf7331 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Parent's Choice |
Version Model Number | K5501US |
Company DUNS | 051957769 |
Company Name | WAL-MART STORES, INC. |
Device Count | 18 |
DM Exempt | false |
Pre-market Exempt | true |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00194346231430 [Primary] |
GS1 | 10194346231437 [Package] Contains: 00194346231430 Package: [2 Units] In Commercial Distribution |
GS1 | 20194346231434 [Package] Package: [2 Units] In Commercial Distribution |
GS1 | 30194346231431 [Unit of Use] |
HHD | Pad, 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 | 2024-11-05 |
Device Publish Date | 2024-10-28 |