Hybrid Guidewire

HYBRID Guidewire is a coiled wire that is designed to fit inside a percutaneous microcatheter for the purpose of directing the catheter through a blood vessel. It is used in association…

Registry build 21.09.26

HYBRID Guidewire is a coiled wire that is designed to fit inside a percutaneous microcatheter for the purpose of directing the catheter through a blood vessel. It is used in association with catheters to enable insertion and easier navigation into the intracranial vascular branches for diagnositc or therapeutic use. Guidewires constitute an important element that conditions the success of the operation. They can be pushed and torqued to move forward through patient’s tortuous anatomy.

10manufacturers in China registered for this device type
5catalogue numbers in this listing

Who Else Makes It

Concentrated in Beijing (4), Jiangsu (3), Guangdong (2). One is registered as a contract manufacturer, able to build to a specification.

Chinese manufacturers registered for FDA product code DQX
Manufacturer City Province Registered as Device types
Mehow Innovative (Huizhou) Ltd. Huizhou Guangdong Contract manufacturer 11
Shanghai JPY ION-Tech Co., Ltd. Shanghai Shanghai Contract manufacturer 70
Suzhou Prosteri Medical Technology Co., Ltd. Suzhou Jiangsu Contract manufacturer 20
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Lepu Medical Technology (Beijing) Co., Ltd. Beijing Beijing Manufacturer 7
Beijing Target Medical Technologies Inc. Beijing Beijing Contract manufacturer 7
Suzhou Zenith Vascular Scitech Limited Suzhou Jiangsu Manufacturer 6
Beijing Bywave Sensing Medical Technology Co., Ltd. Beijing Beijing Manufacturer 2
Shanghai Achieva Medical Suzhou Co., Ltd. Suzhou Jiangsu Manufacturer 2
Deepintec Scientific Co., Ltd. Beijing Beijing Manufacturer 2

Record

Regulatory record for Hybrid Guidewire
Listed by Balt USA, LLC, United States
FDA product code DQX
Device type Wire, Guide, Catheter
Device class Class 2
Regulation 21 CFR 870.1330
Establishment Complaint-file establishment, Manufacturer
510(k) K182337
Record published 2018-12-01

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date
Storage Special storage condition: Store in a dry place at room temperature and away from light

Catalogue Numbers

Catalogue numbers for Hybrid Guidewire
Catalogue number Size Status
HYBRID007D 0.007mm x 220cm In distribution
HYBRID008D 0.008mm x 220cm In distribution
HYBRID007D.120 0.007mm x 120cm In distribution
HYBRID10D300 0.010mm x 310cm In distribution
HYBRID1214DA 0.012mm x 200cm In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Arrow Teleflex Medical LLC 625
Cook Cook Incorporated 410
Guidewire Argon Medical Devices, Inc. 173
Medline Industries, Inc. Medline Industries, Inc. 151
Guidewire Galt Medical Corp. 144
Amplatz Cook Incorporated 128
InQwire® Merit Medical Systems, Inc. 120
Angiographic Guide Wire Medtronic, Inc. 94
Glidewire Terumo Corp. 83
Starter™ Guidewire Lake Region Medical Limited 82
INT,Falcon Guide Wire Shanghai Kindly Medical Instruments Co., Ltd. 72
GuideRight™ St. Jude Medical 69

Showing 12 of 525. All products under Wire, Guide, Catheter

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer