LUMISCOPE

GUDID M368100510LA1

Aneroid manual sphygmomanometer

Primary Device ID	M368100510LA1
NIH Device Record Key	8963d56a-a45e-4014-857e-cbb3cea3272a
Commercial Distribution Status	In Commercial Distribution
Brand Name	LUMISCOPE
Version Model Number	100-510LA
Company DUNS	132016168
Company Name	GF HEALTH PRODUCTS, INC.
Device Count	1
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	false
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
HIBCC	M368100510LA1 [Primary]
HIBCC	M368100510LA2 [Package] Package: [24 Units] In Commercial Distribution

DXQ	Blood Pressure Cuff

Steralize Prior To Use	false
Device Is Sterile	false

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M36811333	Automatic Blood Pressure Monitor
M3682040061	#NURSES STETH BLUE LOT#
M36867003	Portable Ultrasonic Nebulizer
M36811431	Automatic Wrist Blood Pressure Monitor
M368100510LA1	Deluxe Aneroid Blood Pressure Monitor
M3681005101	Deluxe Aneroid Blood Pressure Monitor
M368100040P1	Aneroid Blood Pressure Monitor
M368100040ORC1	Aneroid Blood Pressure Monitor
M368100040HG1	Aneroid Blood Pressure Monitor
M368100040GRP1	Aneroid Blood Pressure Monitor
M368100040DB1	Aneroid Blood Pressure Monitor
M368100040BUR1	Aneroid Blood Pressure Monitor
M368100040BK1	Aneroid Blood Pressure Monitor
M368100001N1	Aneroid Sphygmomanometer
M3681000011	Aneroid Sphygmomanometer

Mark Image Registration \| Serial	Company Trademark Application Date
LUMISCOPE 76303432 2631187 Live/Registered	GF HEALTH PRODUCTS, INC. 2001-08-23
LUMISCOPE 73443255 1360572 Dead/Cancelled	WOBBOT INTERNATIONAL LIMITED 1983-09-12