CROSSLOOP

GUDID 14547327155370

Peripheral vascular guidewire, manual

Primary Device ID	14547327155370
NIH Device Record Key	e640aa94-7fcf-4bb2-aeaf-acca44348a37
Commercial Distribution Status	In Commercial Distribution
Brand Name	CROSSLOOP
Version Model Number	LPM01823S
Company DUNS	690711189
Company Name	ASAHI INTECC CO., LTD.
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

Device Issuing Agency	Device ID
GS1	04547327155373 [Primary]
GS1	14547327155370 [Package] Contains: 04547327155373 Package: [5 Units] In Commercial Distribution

DQX	Wire, guide, catheter

Steralize Prior To Use	false
Device Is Sterile	true

Mark Image Registration \| Serial	Company Trademark Application Date
CROSSLOOP 87410557 5441841 Live/Registered	THE HIRA COMPANY LIMITED 2017-04-13
CROSSLOOP 79383038 not registered Live/Pending	ASAHI INTECC CO., LTD. 2023-09-25
CROSSLOOP 77333950 3467039 Dead/Cancelled	AVG NETHERLANDS B.V. 2007-11-20
CROSSLOOP 77330383 4029058 Dead/Cancelled	AVAST SOFTWARE B.V. 2007-11-15
CROSSLOOP 77328533 3857243 Dead/Cancelled	AVAST SOFTWARE B.V. 2007-11-13
CROSSLOOP 77328528 3648288 Dead/Cancelled	AVG NETHERLANDS B.V. 2007-11-13