Haemolance Plus, safety lancet 7366

GUDID 85907506237071

Blood lancet, single-use

Primary Device ID	85907506237071
NIH Device Record Key	b6a8e6ae-5e9d-4416-acb6-512bbdd19883
Commercial Distribution Status	In Commercial Distribution
Brand Name	Haemolance Plus, safety lancet
Version Model Number	Normal Flow, 21G 1.8mm
Catalog Number	7366
Company DUNS	422528088
Company Name	HTL STREFA S A
Device Count	25
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	false
Expiration Date	true
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	true
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	05907506237075 [Primary]
GS1	15907506237072 [Package] Contains: 05907506237075 Package: Shipper box [45 Units] In Commercial Distribution
GS1	85907506237071 [Unit of Use]

FMK	Lancet, Blood

Steralize Prior To Use	false
Device Is Sterile	true

85907506237941	Safety lancets are sterile, single use medical devices intended for capillary blood sampling.
85907506237071	Safety lancets are sterile, single use medical devices intended for capillary blood sampling.