MedtLancet 30-22-2618

GUDID M992302226185

Manual blood lancing device, single-use

Primary Device ID	M992302226185
NIH Device Record Key	cd3536f4-a42c-46c3-a7ea-d5cb7f18327e
Commercial Distribution Status	In Commercial Distribution
Brand Name	MedtLancet
Version Model Number	1
Catalog Number	30-22-2618
Company DUNS	065756949
Company Name	Carelife (usa) Inc.
Device Count	100
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	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
HIBCC	M992302226180 [Unit of Use]
HIBCC	M992302226183 [Primary]
HIBCC	M992302226185 [Package] Contains: M992302226183 Package: corrugate carton [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

M992302228185	Safety lancet 28G*1.8mm
M992302226185	Safety lancet 26G*1.8mm