AXS Lift LIFT074115-01

GUDID 07613327623390

Vascular guide-catheter, single-use

Primary Device ID	07613327623390
NIH Device Record Key	882f996d-eb70-4b34-95fe-e233b6a91dc2
Commercial Distribution Status	In Commercial Distribution
Brand Name	AXS Lift
Version Model Number	LIFT074115-01
Catalog Number	LIFT074115-01
Company DUNS	042405446
Company Name	Stryker Corporation
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(855)916-3876
Email	NVCustomerService@stryker.com
Phone	+1(855)916-3876
Email	NVCustomerService@stryker.com
Phone	+1(855)916-3876
Email	NVCustomerService@stryker.com

Special Storage Condition, Specify	Between 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool, dry, dark place.
Special Storage Condition, Specify	Between 0 and 0 *Store in a cool, dry, dark place.

Device Issuing Agency	Device ID
GS1	07613327623390 [Primary]

DQY	Catheter, percutaneous

Steralize Prior To Use	false
Device Is Sterile	true