Primary Device ID | 20862850000319 |
NIH Device Record Key | 315f94ed-3702-43fa-bf76-553116b4ec58 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pharmacist Choice |
Version Model Number | Alcohol Prep Pad 100ct |
Company DUNS | 004135503 |
Company Name | SIMPLE DIAGNOSTICS INC |
Device Count | 100 |
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 | true |
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 | 00862850000315 [Primary] |
GS1 | 20862850000319 [Unit of Use] |
LKB | Pad, Alcohol, Device Disinfectant |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-09 |
Device Publish Date | 2020-09-01 |
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