KASM

GUDID 00822409007561

Orthopaedic cement spacer mould Orthopaedic cement spacer mould

Primary Device ID	00822409007561
NIH Device Record Key	a45655b0-5490-4c35-b1fa-650ffdb90d50
Commercial Distribution Status	In Commercial Distribution
Brand Name	KASM
Version Model Number	669-1067
Company DUNS	876542390
Company Name	Ortho Development Corporation
Device Count	1
DM Exempt	true
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

Device Issuing Agency	Device ID
GS1	00822409007561 [Primary]

MBB	BONE CEMENT, ANTIBIOTIC

Steralize Prior To Use	false
Device Is Sterile	true

00822409007608	Large 52A/P x 81M/L Tibial Spacer Mold
00822409007592	Medium 45A/P x 70M/L Tibial Spacer Mold
00822409007585	Small 39A/P x 58M/L Tibial Spacer Mold
00822409007578	Large 53A/P x 75M/L Femoral Spacer Mold
00822409007561	Medium 44A/P x 67M/L Femoral Spacer Mold
00822409007554	Small 37A/P x 60M/L Femoral Spacer Mold

Mark Image Registration \| Serial	Company Trademark Application Date
KASM 85052135 3992272 Live/Registered	Ortho Development Corporation 2010-06-01