20-8000-010-52

GUDID 00889024304710

Surgical drill guide, reusable

Primary Device ID	00889024304710
NIH Device Record Key	bf211229-6e6f-44c7-a37e-e84fb5679b01
Commercial Distribution Status	In Commercial Distribution
Version Model Number	20-8000-010-52
Catalog Number	20-8000-010-52
Company DUNS	205670032
Company Name	Orthosoft Inc
Device Count	1
DM Exempt	false
Pre-market Exempt	false
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	false
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

Phone	1(800)-348-2759
Email	zimmer.consumerrelations@zimmer.com

Device Issuing Agency	Device ID
GS1	00889024304710 [Primary]

HAW	Neurological Stereotaxic Instrument

Steralize Prior To Use	true
Device Is Sterile	false

[00889024304710]

Moist Heat or Steam Sterilization