QEVO

GUDID 04049539072122

Carl Zeiss Meditec AG

Rigid optical neuroscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable Rigid optical intracranial/spinal endoscope, reusable

Primary Device ID	04049539072122
NIH Device Record Key	4d2e037a-2c7a-49d8-a734-21e3eb8a39fc
Commercial Distribution Status	In Commercial Distribution
Brand Name	QEVO
Version Model Number	7212
Company DUNS	342228620
Company Name	Carl Zeiss Meditec AG
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	MR Unsafe
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 Identifiers

Device Issuing Agency	Device ID
GS1	04049539072122 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K170667

FDA Product Code

GWG	Endoscope, Neurological