Full Power AED

Adhesive Medical Device to remove chest hair before defibrillation

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

Who Else Makes It

All of them in Guangdong. 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code LDD
Manufacturer City Province Registered as Device types
Amphenol Medical Technologies (Dongguan) Co., Ltd. Dongguan Guangdong Contract manufacturer 77
Amphenol Alden Products Company Shenzhen Guangdong Contract manufacturer 24
EMI (Dongguan) Asia Limited Dongguan Guangdong Contract manufacturer 9

Record

Regulatory record for Full Power AED
Listed by Full Power Aed, United States
FDA product code LDD
Device type Dc-Defibrillator, Low-Energy, (Including Paddles)
Device class Class 2
Regulation 21 CFR 870.5300
510(k) K150349
Record published 2017-04-12
Record revised 2019-10-23 (version 4)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date, manufacturing date, serial number
Sizes Width 5.872 in; height 7.95 in

Catalogue Numbers

Catalogue numbers for Full Power AED
Catalogue number Size Status
Rapid Hair Removal Pads Width 5.872 in In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Unipower Unipower Corp. 623
Internal Handle Zoll Medical Corporation 89
Vermed Nissha Medical Technologies Limited 47
Cardio Clear Cardio Medical Products, Inc. 33
Dc-Defibrillator, Low-Energy, (Including Paddles) Fiab SPA 20
Dc-Defibrillator, Low-Energy, (Including Paddles) Physio-Control, Inc. 20
R2 ConMed Corporation 17
HeartStart Philips Medical Systems Hsg 9
Anybattery Anybattery, Inc 6
Tempus LS-Manual Remote Diagnostic Technologies Ltd. 6
Vermed Defib Pads Graphic Controls Acquisition Corporation 5
HeartStart Philips Electronics North America Corporation 4

Showing 12 of 29. All products under Dc-Defibrillator, Low-Energy, (Including Paddles)

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K150349 2015-07-14

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