Identity
- Trade Name
- HeartStart Pads FDA UDI
- Generic Name
- External defibrillation electrode, adult, single-use FDA UDI
- Device Name
- HeartStart Adult Radiotransparent Pads FDA UDI
- Model / Reference
- 989803125401 FDA UDI
- Description
- HeartStart Adult Radiotransparent Pads FDA UDI
Identifiers
- Catalog Number
- M3718A FDA UDI
- Primary DI / UDI-DI
- 00884838002876 FDA UDI
- FDA Product Code
- MKJ FDA UDI
- GMDN Term
- External defibrillation electrode, adult, single-use FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.5310 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: External defibrillation electrode, adult, single-use
HeartStart Pads by Philips Medical Systems Hsg — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as External defibrillation electrode, adult, single-use.
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- Powerheart® Adult Defibrillation Pads — Zoll Medical Corporation · Class III
- Cardio Clear — CARDIO MEDICAL PRODUCTS, INC. · Class II
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- Intellisense Adult Defibrillation Pads, CPR Device, Powerheart® G5 — Cardiac Science Corporation · Class III
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class III | Pending data |
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Manufacturer
- Manufacturer
- Philips Medical Systems Hsg
Sources (1)
- FDA UDI 1cee1d1a-a946-426b-b24f-4c14eecb8010 34 fields · synced May 30, 2026