OSMETTE III 5010F

GUDID 00850041049847

Osmometric analyser IVD

Primary Device ID	00850041049847
NIH Device Record Key	a785d9a0-3161-4015-8c86-0cc1a746e7c7
Commercial Distribution Status	In Commercial Distribution
Brand Name	OSMETTE III
Version Model Number	5010F
Catalog Number	5010F
Company DUNS	001001676
Company Name	Precision Systems, Inc.
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	true
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	00850041049847 [Primary]

JJM	Osmometer For Clinical Use

Steralize Prior To Use	false
Device Is Sterile	false

00850041049847	Precision Systems OSMETTE III osmometer, 220 V
00850041049823	Precision Systems OSMETTE III osmometer, 110 V