Cordis

7F HF 0.038 Inches 110CM 12SH PIG145

Registry build 21.09.26
11manufacturers in China registered for this device type
77catalogue numbers in this listing
29510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (5), Guangdong (3), Zhejiang (2). 4 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DQO
Manufacturer City Province Registered as Device types
GE Medical Systems (China) Co., Ltd. Wuxi Jiangsu Contract manufacturer 57
Amsino Medical (Kunshan) Co., Ltd. Kunshan Jiangsu Contract manufacturer 53
Conod Medical Shuyang Co., Ltd. Shuyang Jiangsu Contract manufacturer 22
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8
GRI Medical & Electronic Technology Co., Ltd. Jiaxing Zhejiang Contract manufacturer 71
Goals Sterilization Co., Ltd. Jiaxing Zhejiang Contract manufacturer 26
Wuxi Goals Medical Technology Co., Ltd. Yixing Jiangsu Contract manufacturer 24
Sunny Medical Device (Shenzhen) Co., Ltd. Shenzhen Guangdong Contract manufacturer 11
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Shenzhen Vivolight Medical Device&Technology Co., Ltd. Shenzhen Guangdong Manufacturer 4
Shenzhen Antmed Co., Ltd. Dongguan Guangdong Manufacturer 4

Record

Regulatory record for Cordis
Listed by Cordis Corp., United States
FDA product code DQO
Device type Catheter, Intravascular, Diagnostic
Device class Class 2
Regulation 21 CFR 870.1200
510(k) K862006
Record published 2016-08-01
Record revised 2024-08-09 (version 7)

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
Packaging Box of 5, box of 3
Distribution end date 2024-08-08

Catalogue Numbers

Catalogue numbers for Cordis
Catalogue number Size Status
67000000 In distribution
CP0175 In distribution
67001000 In distribution
533545 In distribution
SR1414 Withdrawn
SR0774 Withdrawn
SR4057 Withdrawn
SR1489 Withdrawn
SRD6980 Withdrawn
SRD6652 Withdrawn
SRD5633 Withdrawn
MODC12580 Withdrawn
HF7LP145 Withdrawn
SR1415 Withdrawn
MODC18351 Withdrawn
MODC18462 Withdrawn
SRD6030 Withdrawn
SRD5931 Withdrawn
SRD5660 Withdrawn
MODC16934 Withdrawn
SR3888 Withdrawn
SR4319 Withdrawn
SRD6743 Withdrawn
MODC16645 Withdrawn
MODC10581 Withdrawn
MODC18558 Withdrawn
SR2546 Withdrawn
MODC18197 Withdrawn
MODC17831 Withdrawn
SRD6704 Withdrawn
SR0950 Withdrawn
SR0806 Withdrawn
SRD6631 Withdrawn
SR1413 Withdrawn
SRD5652 Withdrawn
MODC16899 Withdrawn
SR3602 Withdrawn
SR2006 Withdrawn
MODC18041 Withdrawn
SRD6665 Withdrawn
MODC17987 Withdrawn
MODC02775 Withdrawn
MODC15105 Withdrawn
SR3457 Withdrawn
SR1511 Withdrawn
MODC18126 Withdrawn
MODC02039 Withdrawn
SR3625 Withdrawn
SR0654 Withdrawn
SRD6825 Withdrawn
MODC14012 Withdrawn
MODC17772 Withdrawn
MODC18131 Withdrawn
SR3360 Withdrawn
MODC17996 Withdrawn
SRD5678 Withdrawn
SRD5873 Withdrawn
SRD6860 Withdrawn
SR2059 Withdrawn
MODC18074 Withdrawn
MODC13112 Withdrawn
MODC15345 Withdrawn
SR0659 Withdrawn
SRD5659 Withdrawn
SR2170 Withdrawn
MODC18303 Withdrawn
MODC02776 Withdrawn
SR1814 Withdrawn
SR0997 Withdrawn
SRD6045 Withdrawn
SR2547 Withdrawn
SRD5631 Withdrawn
SR3150 Withdrawn
MODC17886 Withdrawn
SR0854 Withdrawn
MODC17872 Withdrawn
SR2169 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Performa® Merit Medical Systems, Inc. 1,101
Impress® Merit Medical Systems, Inc. 839
Super Torque Cordis Corp. 611
Soft-Vu AngioDynamics, Inc. 591
Torcon NB Cook Incorporated 463
Mariner AngioDynamics, Inc. 323
INT,SlideCath Shanghai Kindly Medical Instruments Co., Ltd. 264
Infiniti Cordis Corp. 251
Infiniti Cordis US Corp. 241
AngiOptic AngioDynamics, Inc. 227
Tempo Cordis Corp. 217
SiteSeer™ Medtronic, Inc. 204

Showing 12 of 226. All products under Catheter, Intravascular, Diagnostic

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K212977 2022-02-17
K020316 2002-03-20
K000579 2000-05-03
K992347 1999-10-08
K991673 1999-05-26
K973401 1997-11-18
K970854 1997-09-30
K971646 1997-07-14
K962759 1996-10-10
K960975 1996-04-02
K942939 1994-08-31
K936260 1994-05-31
K922891 1993-06-23
K930479 1993-04-21
K921310 1992-09-17
K915498 1992-04-17
K915836 1992-02-11
K914141 1991-10-23
K914007 1991-10-18
K911703 1991-06-28
K905297 1991-02-01
K896308 1990-03-28
K872248 1987-08-12
K864141 1986-11-03
K862244 1986-08-25
K862006 1986-06-27
K854576 1986-02-26
K844161 1985-01-02
K802629 1980-10-31

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