Saber

Saber 6MM3CM 150

Registry build 21.09.26
5manufacturers in China registered for this device type
1catalogue number

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 Saber
Listed by Cordis Cashel
FDA product code LIT
Device type Catheter, Angioplasty, Peripheral, Transluminal
Device class Class 2
Regulation 21 CFR 870.1250
510(k) K133843
Record published 2016-10-27
Record revised 2026-01-26 (version 9)

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
Distribution end date 2026-01-23

Catalogue Numbers

Catalogue numbers for Saber
Catalogue number Size Status
48006003X Withdrawn

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

Recalls Naming This Product

1 recall names this product by its own identifier, the 510(k) it is cleared under.

Recalls naming the identifiers of Saber
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
Cordis US Corp. 510(k) number 2021-07-19 Class II Under Investigation by firm The balloon protective sheath may potentially be contaminated with a foreign material left over from the manufacturing process. The contaminant may transfer over from the sheath to the balloon. 8 units 2023-02-16

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