Advance Micro

Advance Micro 14 Ultra Low-Profile PTA Balloon Catheter

Registry build 21.09.26
5manufacturers in China registered for this device type
69catalogue numbers in this listing
13510(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 Advance Micro
Listed by Cook Incorporated, United States
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
Establishment Contract manufacturer, Contract steriliser, Specification developer, Complaint-file establishment, Manufacturer, Exporter
Record published 2016-09-24
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
Storage Special storage condition: Store in dark, dry, cool place.

Catalogue Numbers

Catalogue numbers for Advance Micro
Catalogue number Size Status
G26403 In distribution
G26101 In distribution
G26608 In distribution
G26604 In distribution
G26678 In distribution
G26119 In distribution
G26118 In distribution
G26106 In distribution
G26724 In distribution
G26098 In distribution
G26122 In distribution
G26400 In distribution
G26112 In distribution
G26710 In distribution
G26099 In distribution
G26406 In distribution
G26115 In distribution
G26646 In distribution
G26094 In distribution
G26626 In distribution
G26195 In distribution
G26096 In distribution
G26605 In distribution
G26104 In distribution
G26665 In distribution
G26625 In distribution
G26610 In distribution
G26614 In distribution
G26090 In distribution
G26641 In distribution
G26620 In distribution
G26606 In distribution
G26621 In distribution
G26680 In distribution
G26100 In distribution
G26107 In distribution
G26405 In distribution
G26117 In distribution
G26402 In distribution
G26404 In distribution
G26622 In distribution
G26677 In distribution
G26103 In distribution
G26602 In distribution
G26681 In distribution
G26121 In distribution
G26643 In distribution
G26636 In distribution
G26611 In distribution
G26607 In distribution
G26407 In distribution
G26653 In distribution
G26093 In distribution
G26679 In distribution
G26102 In distribution
G26123 In distribution
G26401 In distribution
G26601 In distribution
G26092 In distribution
G26095 In distribution
G26111 In distribution
G26706 In distribution
G26105 In distribution
G26707 In distribution
G26719 In distribution
G26110 In distribution
G26091 In distribution
G26109 In distribution
G26113 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
K170193 2017-02-13
K132020 2013-10-25
K130293 2013-05-31
K113300 2011-12-09
K023504 2002-11-13
K001087 2000-07-20
K980390 1998-08-20
K981906 1998-06-29
K972800 1998-04-16
K924358 1993-05-20
K900677 1991-02-22
K882052 1988-09-14
K870215 1987-08-12

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