MediGuide¿™ MG1000

GUDID 05415067018519

Cardiac mapping system

Primary Device ID	05415067018519
NIH Device Record Key	449bcefd-a0e8-410e-b469-3a1b16123214
Commercial Distribution Status	In Commercial Distribution
Brand Name	MediGuide¿™
Version Model Number	Technology
Catalog Number	MG1000
Company DUNS	149818952
Company Name	ST. JUDE MEDICAL, 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	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	true
OTC Over-The-Counter	false

Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.
Special Storage Condition, Specify	Between 0 and 0 *Keep dry. Do not use if package is damaged.

Device Issuing Agency	Device ID
GS1	05415067018519 [Primary]

DQK	COMPUTER, DIAGNOSTIC, PROGRAMMABLE

Steralize Prior To Use	false
Device Is Sterile	false