ProVia 9

GUDID 20643169453047

Cardiac/peripheral vascular guidewire, single-use Cardiac/peripheral vascular guidewire, single-use

Primary Device ID	20643169453047
NIH Device Record Key	54c3cb17-de7d-4444-83d9-c0b7257282b9
Commercial Distribution Status	In Commercial Distribution
Brand Name	ProVia 9
Version Model Number	9PROV180SS
Company DUNS	006261481
Company Name	MEDTRONIC, 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	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 *Store in a cool, dark, dry place. Do not expose to organic solvents.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool, dark, dry place. Do not expose to organic solvents.

Device Issuing Agency	Device ID
GS1	00643169453043 [Primary]
GS1	20643169453047 [Package] Contains: 00643169453043 Package: PK [5 Units] In Commercial Distribution

DQX	WIRE, GUIDE, CATHETER

Steralize Prior To Use	false
Device Is Sterile	true