Progreat

PROGREAT Microcatheter Coaxial System

Registry build 21.09.26
11manufacturers in China registered for this device type
18catalogue numbers in this listing
9510(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 Progreat
Listed by Terumo Corp., Japan
FDA product code DQO
Device type Catheter, Intravascular, Diagnostic
Device class Class 2
Regulation 21 CFR 870.1200
Establishment Contract manufacturer, Contract steriliser, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter
Record published 2017-09-07
Record revised 2019-03-21 (version 3)

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
Storage Special storage condition: Fragile. Keep dry. Keep away from sunlight. Stacking limit by 10.
Packaging Carton of 5, pack of 5
Sizes Length 110 to 150 cm; outer diameter 0.67 to 0.93 mm; lumen/inner diameter 0.49 to 0.7 mm

Catalogue Numbers

Catalogue numbers for Progreat
Catalogue number Size Status
MC*PP28151YV Clinically Relevant Size 1 is relative to catheter distal end. And other Clinically Relevant Sizes are relative to catheter shaft. In distribution
MC*PC2015Y Outer Diameter 0.67 mm In distribution
MC*PB2811Y Length 110 cm In distribution
MC*PP24151YW Outer Diameter 0.8 mm In distribution
MC*PC2015ZRC Lumen/Inner Diameter 0.49 mm In distribution
MC*PE24131YB Length 130 cm In distribution
MC*PE28131YB Clinically Relevant Size 1 is relative to catheter distal end. And other Clinically Relevant Sizes are relative to catheter shaft. In distribution
MC*PV2415Y Clinically Relevant Size 1 is relative to catheter distal end. And other Clinically Relevant Sizes are relative to catheter shaft. In distribution
MC*PB2413Y Outer Diameter 0.80 mm In distribution
MC*PC2011Y Length 110 cm In distribution
MC*PC2713Y Length 130 cm In distribution
MC*PE24111YB Clinically Relevant Size 1 is relative to catheter distal end. And other Clinically Relevant Sizes are relative to catheter shaft. In distribution
MC*PC2015ZRA Outer Diameter 0.67 mm In distribution
MC*PE28151YV Lumen/Inner Diameter 0.70 mm In distribution
MC*PE24151YV Length 150 cm In distribution
MC*PE27111Y Outer Diameter 0.90 mm In distribution
MC*PB2413ZRC Length 130 cm In distribution
MC*PP27151Y Lumen/Inner Diameter 0.65 mm In distribution

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
K250751 2025-07-17
K113335 2012-07-16
K092372 2009-09-11
K090040 2009-02-06
K082736 2008-09-24
K033583 2003-12-12
K992051 1999-08-10
K915414 1992-02-04
K863137 1986-10-10

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