Unistik Pro

GUDID 00384701634031

Manual blood lancing device, single-use

Primary Device ID	00384701634031
NIH Device Record Key	e45dfa3a-6b2b-4575-89b4-994455f1b4b3
Commercial Distribution Status	In Commercial Distribution
Brand Name	Unistik Pro
Version Model Number	AT 1634
Company DUNS	217266915
Company Name	OWEN MUMFORD LIMITED
Device Count	200
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	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	true
OTC Over-The-Counter	true

Device Issuing Agency	Device ID
GS1	00384701634000 [Unit of Use]
GS1	00384701634017 [Primary]
GS1	00384701634031 [Package] Contains: 00384701634017 Package: Case [20 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

00384701644030	Unistik Pro Safety Lancet - 28G x 1.2mm
00384701634031	Unistik Pro Safety Lancet - 25G x 1.6mm
00384701614033	Unistik Pro Safety Lancet - 21G x 2.0mm