ZevRx Twist Top Lancets 30G

GUDID 10850632007765

Manual blood lancing device, single-use

Primary Device ID	10850632007765
NIH Device Record Key	d73060e5-83c3-41d3-b02a-08833eda5fdb
Commercial Distribution Status	In Commercial Distribution
Brand Name	ZevRx Twist Top Lancets 30G
Version Model Number	1
Company DUNS	783518983
Company Name	HOME AIDE DIAGNOSTICS, INC.
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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	true
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	00850632007768 [Primary]
GS1	10850632007765 [Package] Contains: 00850632007768 Package: Case [200 Units] In Commercial Distribution

FMK	Single Use Only Blood Lancet With An Integral Sharps Injury Prevention Feature

Steralize Prior To Use	false
Device Is Sterile	true

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