Bipolar Pacing Catheter

Catalogue number BP2502-10, listed by Bioptimal International Pte. Ltd., Singapore, under Electrode, Pacemaker, Temporary. 3 manufacturers in China are registered for this product code.

Registry build 21.09.26
3manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

Concentrated in Guangdong (2), Shandong (1).

Chinese manufacturers registered for FDA product code LDF
Manufacturer City Province Registered as Device types
Dongguan King Medical Technology Co., Ltd. Dongguan Guangdong Contract manufacturer 14
Shenzhen Launch Electrical Co., Ltd. Shenzhen Guangdong Contract manufacturer 8
Bioxin Medical Co., Ltd. Weihai Shandong Contract manufacturer 8

Record

Regulatory record for Bipolar Pacing Catheter
Listed by Bioptimal International Pte. Ltd., Singapore
FDA product code LDF
Device type Electrode, Pacemaker, Temporary
Device class Class 2
Regulation 21 CFR 870.3680
Establishment Manufacturer
Record published 2026-05-04

Specifications

Specifications
MRI safety MR Unsafe
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Latex Contains natural rubber latex
Label carries lot or batch number, expiry date, manufacturing date
Storage Storage environment humidity 10 to 85 % RH; Storage environment temperature 4 to 35 °C; Special storage condition: Bioptimal Bipolar Pacing Catheters should be stored unopened in its original packaging in a normal temperature, well-ven

Catalogue Numbers

Catalogue numbers for Bipolar Pacing Catheter
Catalogue number Size Status
BP2502-10 In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
MYO/Wire® Ultra-Thin Temporary Pacing Wires A & E Medical Corporation 109
Myo/Wire A & E Medical Corporation 76
TB Oscor Inc. 40
Temporary Myocardial Heartwire Oscor Inc. 27
Pacel™ St. Jude Medical Cardiovascular Division 16
Ethicon Ethicon, Inc. 15
Flexon Covidien LP 13
Electrode, Pacemaker, Temporary Medtronic, Inc. 12
Nbih™ Temporary Pacing Electrode Catheter C.R. Bard, Inc. 11
Electrode, Pacemaker, Temporary C.R. Bard, Inc. 10
Streamline™ Medtronic, Inc. 10
Steelex B Braun Surgical SA 9

Showing 12 of 31. All products under Electrode, Pacemaker, Temporary

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K242863 2025-06-15

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