Primary Device ID | 30370797780999 |
NIH Device Record Key | d32312f1-cdef-41c7-9e21-ae543bc49520 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dr Talbot's |
Version Model Number | 78099 |
Company DUNS | 078855555 |
Company Name | TALBOT'S PHARMACEUTICALS FAMILY PRODUCTS, LLC |
Device Count | 1 |
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 | false |
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 | 00370797780998 [Primary] |
GS1 | 20370797780992 [Package] Contains: 00370797780998 Package: [4 Units] In Commercial Distribution |
GS1 | 30370797780999 [Package] Contains: 00370797780998 Package: [16 Units] In Commercial Distribution |
PWX | Insect Sting Emergency Kit |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-08-12 |
Device Publish Date | 2024-08-02 |