HEINE GAMMA® XXL LF M-000.09.323

GUDID 04053755190690

Aneroid manual sphygmomanometer

Primary Device ID	04053755190690
NIH Device Record Key	d0bb5507-9074-429e-b15f-2a83f85e68eb
Commercial Distribution Status	In Commercial Distribution
Brand Name	HEINE GAMMA® XXL LF
Version Model Number	166
Catalog Number	M-000.09.323
Company DUNS	315274563
Company Name	Heine Optotechnik GmbH & Co. KG
Device Count	1
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	false
Lot Batch	false
Serial Number	false
Manufacturing Date	true
Expiration Date	false
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	04053755190690 [Primary]

DXN	System, Measurement, Blood-Pressure, Non-Invasive

Steralize Prior To Use	false
Device Is Sterile	false