Refraction Unit

GUDID 05907642694442

Ophthalmic examination station

Primary Device ID	05907642694442
NIH Device Record Key	a97813af-6f27-4d0d-b7ae-f4b2790c3d8c
Commercial Distribution Status	In Commercial Distribution
Brand Name	Refraction Unit
Version Model Number	UNIQ
Company DUNS	366126408
Company Name	MDT SP Z O O
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	false
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	05907642694442 [Primary]

HMF	Stand, Instrument, Ac-Powered, Ophthalmic

Steralize Prior To Use	false
Device Is Sterile	false