Primary Device ID | 10891237001178 |
NIH Device Record Key | 0b0e28af-0a81-4be5-846b-1ea94835ab4d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Easy Mini Eject Lancing Device |
Version Model Number | LF-LDE |
Catalog Number | 1171 |
Company DUNS | 783518983 |
Company Name | HOME AIDE DIAGNOSTICS, 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 | 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 |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us | |
Phone | 18009150116 |
info@homeaide.us |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00891237001171 [Primary] |
GS1 | 10891237001178 [Package] Contains: 00891237001171 Package: Outer Case [100 Units] In Commercial Distribution |
FMK | Lancet, Blood |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2022-11-29 |
Device Publish Date | 2018-08-03 |
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