Polaris 5.5 Spinal System

GUDID 00880304876255

CURVED THORACIC PROBE, LARGE

ZIMMER BIOMET INC

Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable Abdominal/ENT/orthopaedic surgical probe, reusable

Primary Device ID	00880304876255
NIH Device Record Key	76e456f5-0df3-4f27-8cfa-6e2ac9d886c5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Polaris 5.5 Spinal System
Version Model Number	14-500137
Company DUNS	045576443
Company Name	ZIMMER BIOMET 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	true
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	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00880304876255 [Primary]

FDA Product Code

HXB

Probe