Droplet Acti-Lance, safety lancets 9630

GUDID 15903999602274

Blood lancet, single-use

Primary Device ID	15903999602274
NIH Device Record Key	99f17b3b-88a1-4162-b251-0816c4959106
Commercial Distribution Status	In Commercial Distribution
Brand Name	Droplet Acti-Lance, safety lancets
Version Model Number	28G x 1.5mm
Catalog Number	9630
Company DUNS	422528088
Company Name	HTL STREFA S A
Device Count	50
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	false
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	05903999602277 [Primary]
GS1	15903999602274 [Package] Contains: 05903999602277 Package: shipper box [24 Units] In Commercial Distribution
GS1	85903999602273 [Unit of Use]

FMK	Lancet, Blood

Steralize Prior To Use	false
Device Is Sterile	true

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