Pedi-Padz

Pedi*padz Pacing Only Pediatric Electrodes - 1 Pair

Registry build 21.09.26
2manufacturers in China registered for this device type
1catalogue number
1510(k) clearance

Who Else Makes It

All of them in Guangdong. 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code DRO
Manufacturer City Province Registered as Device types
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9

Record

Regulatory record for Pedi-Padz
Listed by Zoll Medical Corporation, United States
FDA product code DRO
Device type Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)
Device class Class 2
Regulation 21 CFR 870.5550
Establishment Contract manufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer
Record published 2014-09-24
Record revised 2026-02-16 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Label carries lot or batch number, expiry date
Storage Storage environment temperature 0 to 35 °C; Handling environment temperature 0 to 50 °C
Packaging Case of 6
Distribution end date 2026-01-01

Catalogue Numbers

Catalogue numbers for Pedi-Padz
Catalogue number Size Status
8900-1061 9.0″ X 8.0″ X 1.0″ Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
M Series Biphasic Zoll Medical Corporation 97
Defibrillation Electrodes TZ Medical, Inc. 31
Medi-Trace Cadence Cardinal Health 17
Kendall Cardinal Health 5
R Series Zoll Medical Corporation 5
HeartStart Philips Medical Systems Hsg 2
Pacemaker, Cardiac, External Transcutaneous (Non-Invasive) Philips Medical Systems Hsg 2
PAD 3020-XLT TZ Medical, Inc. 1
PAD 1115Z TZ Medical, Inc. 1
Pad 101NHK TZ Medical, Inc. 1
PAD 1114 TZ Medical, Inc. 1
PAD 3020-HP TZ Medical, Inc. 1

Showing 12 of 36. All products under Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K950856 1995-12-29

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