Primary Device ID | 00189116000163 |
NIH Device Record Key | 4b6f9211-dd58-4695-b3d4-0c6317a872d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Primocyn Eau Divine Skin Solution |
Version Model Number | 84887 |
Catalog Number | 84887 |
Company DUNS | 081642964 |
Company Name | Sonoma Pharmaceuticals, Inc. |
Device Count | 1 |
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 | true |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Total Volume | 500 Milliliter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00189116000163 [Primary] |
GS1 | 20189116000167 [Package] Package: Box [12 Units] In Commercial Distribution |
FRO | Dressing, Wound, Drug |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-12-12 |
Device Publish Date | 2022-12-02 |
00189116000231 | 85003 |
00189116000163 | 84887 |
00189116000156 | 84891 |
00189116000149 | 84890 |