00-5220-065-02

GUDID 00889024187726

Knee arthroplasty wedge

Primary Device ID	00889024187726
NIH Device Record Key	9cda20b5-4c87-4851-bb12-30993243199d
Commercial Distribution Status	In Commercial Distribution
Version Model Number	5220-65-02
Catalog Number	00-5220-065-02
Company DUNS	056038268
Company Name	Zimmer, 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	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	true
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@zimmerbiomet.com

Height

19 Millimeter

Device Issuing Agency	Device ID
GS1	00889024187726 [Primary]

HSX	PROSTHESIS, KNEE, FEMOROTIBIAL, NON-CONSTRAINED, CEMENTED, METAL/POLYMER

Steralize Prior To Use	false
Device Is Sterile	true