First Choice

25 catalogue numbers from UHP7572, listed by Creagh Medical Ltd., Ireland, under Catheter, Angioplasty, Peripheral, Transluminal. 5 manufacturers in China are registered for this product code.

Registry build 21.09.26
5manufacturers in China registered for this device type
25catalogue numbers in this listing
6510(k) clearances naming this product code

Who Else Makes It

Concentrated in Jiangsu (3), Guangdong (2).

Chinese manufacturers registered for FDA product code LIT
Manufacturer City Province Registered as Device types
OrbusNeich Medical (Shenzhen) Co., Ltd. Shenzhen Guangdong Complaint-file establishment 5
Curatia Medical Limited Suzhou Jiangsu Specification developer 5
Brosmed Medical Co., Ltd. Dongguan Guangdong Contract manufacturer 4
Kossel Medtech (Suzhou) Co., Ltd. Suzhou Jiangsu Manufacturer 4
DK Medical Technology Co., Ltd. Suzhou Jiangsu Manufacturer 3

Record

Regulatory record for First Choice
Listed by Creagh Medical Ltd., Ireland
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Contract manufacturer, Complaint-file establishment, Manufacturer
510(k) K102645
Record published 2018-06-05
Record revised 2019-08-09 (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, manufacturing date

Catalogue Numbers

Catalogue numbers for First Choice
Catalogue number Size Status
UHP7572 In distribution
UHP75610 In distribution
UHP7544 In distribution
UHP7556 In distribution
UHP7534 In distribution
EUHP75124 In distribution
EUHP75164 In distribution
UHP7594 In distribution
UHP7586 In distribution
UHP7562 In distribution
UHP7554 In distribution
UHP7542 In distribution
UHP7584s In distribution
UHP7564 In distribution
UHP75104 In distribution
UHP7584 In distribution
UHP7574 In distribution
UHP7588 In distribution
UHP7576 In distribution
UHP7574s In distribution
UHP7582 In distribution
UHP7566 In distribution
UHP7552 In distribution
EUHP75144 In distribution
UHP75710 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Parafleet SC 018 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 1,460
Jade Plus PTA Balloon Dilatation Catheter / Jade Plus 18 OTW OrbusNeich Medical (Shenzhen) Co., Ltd. 832
Jade PTA Balloon Dilatation Catheter OrbusNeich Medical (Shenzhen) Co., Ltd. 667
Parafleet SC 014 PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 572
Minerva PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 504
Advocate Arravasc, Ltd. 441
Ultraverse® 035 PTA Dilatation Catheter Bard Peripheral Vascular, Inc. 361
Polux PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 359
Advance Cook Incorporated 355
Pacific™ Plus Medtronic, Inc. 347
EverCross™ ev3, Inc. 316
Achilles NC PTA Balloon Dilatation Catheter Brosmed Medical Co., Ltd. 297

Showing 12 of 167. All products under Catheter, Angioplasty, Peripheral, Transluminal

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K230191 2023-03-22
K200700 2020-05-14
K180007 2018-04-19
K171251 2017-09-08
K113468 2011-12-20
K102645 2010-12-10

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