OSMETTE XL 5007

GUDID 00850041049755

Osmometric analyser IVD

Primary Device ID	00850041049755
NIH Device Record Key	6affc7f1-6d4b-4f00-b8f8-c1e893440699
Commercial Distribution Status	In Commercial Distribution
Brand Name	OSMETTE XL
Version Model Number	5007
Catalog Number	5007
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	00850041049755 [Primary]

JJM	Osmometer For Clinical Use

Steralize Prior To Use	false
Device Is Sterile	false

00850041049779	Precision Systems OSMETTE XL osmometer, 220 V
00850041049755	Precision Systems OSMETTE XL osmometer, 110 V