CAPIJECT SAFETY LANCET

GUDID 50389701009235

Manual blood lancing device, single-use

Primary Device ID	50389701009235
NIH Device Record Key	fca3ba75-78a4-4f7e-92cb-c2df59c0f59d
Commercial Distribution Status	In Commercial Distribution
Brand Name	CAPIJECT SAFETY LANCET
Version Model Number	200105
Company DUNS	718296825
Company Name	ASAHI POLYSLIDER COMPANY,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	false

Device Issuing Agency	Device ID
GS1	30389701009231 [Primary]
GS1	50389701009235 [Package] Contains: 30389701009231 Package: Cardboard box [10 Units] In Commercial Distribution
GS1	80812608030312 [Unit of Use]

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

Steralize Prior To Use	false
Device Is Sterile	true

50389701009235	Box of 200 Sterile Single-Use Lancing Device Needle 28G
50389701009228	Box of 200 Sterile Single-Use Lancing Device Needle 23G
50389701009211	Box of 200 Sterile Single-Use Lancing Device Blade 2.0
50389701009204	Box of 200 Sterile Single-Use Lancing Device Blade 1.5
80812608030275	Box of 200 Sterile Single-Use Lancing Device Blade 1.0