Ethicon

Temporary Cardiac Pacing Wire

Registry build 21.09.26
3manufacturers in China registered for this device type
15catalogue numbers in this listing
5510(k) clearances naming this product code

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 Ethicon
Listed by Ethicon, Inc., United States
FDA product code LDF
Device type Electrode, Pacemaker, Temporary
Device class Class 2
Regulation 21 CFR 870.3680
Establishment Contract manufacturer, Specification developer, Manufacturer, Exporter
Record published 2015-09-01
Record revised 2024-11-11 (version 7)

Specifications

Specifications
MRI safety MR Conditional
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Packaging Box of 12
Distribution end date 2023-11-15

Catalogue Numbers

Catalogue numbers for Ethicon
Catalogue number Size Status
TPW90 In distribution
TPW72 In distribution
TPW80 In distribution
TPW40 In distribution
TPW10 In distribution
TPW92 In distribution
TPW30 In distribution
TPW70 In distribution
TPW42 In distribution
TPW32 In distribution
D9148 In distribution
TPW20 In distribution
TPW50 Withdrawn
TPW52 Withdrawn
TPW62 Withdrawn

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
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
Helios Oscor Inc. 8

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

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K173923 2018-08-02
K980503 1998-04-10
K822155 1982-08-24
K813138 1981-12-10
K781002 1978-12-04

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