Enhanced Peripheral

32 catalogue numbers from Enhanced Peripheral, 30G 300-018, listed by Brivant, Ltd., Ireland, under Wire, Guide, Catheter. 10 manufacturers in China are registered for this product code.

Registry build 21.09.26
10manufacturers in China registered for this device type
32catalogue numbers in this listing
9510(k) clearances naming this product code

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 Enhanced Peripheral
Listed by Brivant, Ltd., Ireland
FDA product code DQX
Device type Wire, Guide, Catheter
Device class Class 2
Regulation 21 CFR 870.1330
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
Record published 2020-05-15
Record revised 2024-11-27 (version 3)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Supplied sterile Yes
Single use Yes
Label carries lot or batch number, expiry date
Packaging Carton of 5

Catalogue Numbers

Catalogue numbers for Enhanced Peripheral
Catalogue number Size Status
Enhanced Peripheral, 30G 300-018 In distribution
Enhanced Peripheral, 195-25G In distribution
Enhanced Peripheral, 4G 300-014 In distribution
Enhanced Peripheral, 300-18G In distribution
Enhanced Peripheral, 6G 300-018 In distribution
Enhanced Peripheral, 300-25G In distribution
Enhanced Peripheral, 6G 195-014 In distribution
Enhanced Peripheral, 12G 195-018 In distribution
Enhanced Peripheral, 195-12G In distribution
Enhanced Peripheral, 4G 300-018 In distribution
Enhanced Peripheral, 195-25G In distribution
Enhanced Peripheral, 300-12G In distribution
Enhanced Peripheral, 4G 195-018 In distribution
Enhanced Peripheral, 195-18G In distribution
Enhanced Peripheral, 300-30G In distribution
Enhanced Peripheral, 12G 300-014 In distribution
Enhanced Peripheral, 300-12G In distribution
Enhanced Peripheral, 30G 195-018 In distribution
Enhanced Peripheral, 30G 300-014 In distribution
Enhanced Peripheral, 300-30G In distribution
Enhanced Peripheral, 6G 195-018 In distribution
Enhanced Peripheral, 195-18G In distribution
Enhanced Peripheral, 30G 195-014 In distribution
Enhanced Peripheral, 12G 195-014 In distribution
Enhanced Peripheral, 195-30G In distribution
Enhanced Peripheral, 300-18G In distribution
Enhanced Peripheral, 4G 195-014 In distribution
Enhanced Peripheral, 12G 300-018 In distribution
Enhanced Peripheral, 195-12G In distribution
Enhanced Peripheral, 195-30G In distribution
Enhanced Peripheral, 300-25G In distribution
Enhanced Peripheral, 6G 300-014 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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K141831 2014-09-04
K122856 2012-10-17
K120137 2012-02-14
K103377 2011-05-18
K102211 2010-09-03
K093515 2010-02-16
K083094 2009-07-07
K073082 2008-01-09
K060551 2006-06-07

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