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Heartstart Infant Child Smart Pads Cart.
EUDAMEDFDA UDIClass IIb (EU MDR)
Ref M5072AModel Defibrillation Pads Class IIb
Identity
- Trade Name
- Heartstart Infant Child Smart Pads Cart. EUDAMEDPHILIPS HeartStart Infant/Child SMART Pads FDA UDI
- Generic Name
- External defibrillation electrode, paediatric, single-use FDA UDI
- Device Name
- Defibrillation Pads Class IIb EUDAMEDHeartStart Infant/Child SMART Pads Cartridge FDA UDI
- Model / Reference
- Defibrillation Pads Class IIb EUDAMEDM5072A EUDAMEDHeartstart Infant Child Smart Pads Cart. FDA UDI
- Description
- HeartStart Infant/Child SMART Pads Cartridge FDA UDI
Identifiers
- Catalog Number
- M5072A FDA UDI
- Primary DI / UDI-DI
- 00884838127784 EUDAMEDFDA UDI
- Basic UDI-DI
- 0884838BM1736MZ EUDAMED
- FDA Product Code
- MKJ FDA UDI
- EMDN Code
- Z12030585 DEFIBRILLATORS - CONSUMABLES EUDAMED
- GMDN Term
- External defibrillation electrode, paediatric, single-use FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass III FDA UDI
- Regulation Number
- 870.5310 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
Yes
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
No
EUDAMED
Contains Latex
No
EUDAMEDFDA UDI
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Prescription Use
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Heartstart Infant Child Smart Pads Cart. by Philips Medical Systems — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDR
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDR | 0884838BM1736MZ | Class IIb | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIb | Pending data |
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Manufacturer
- Manufacturer
- Philips Medical Systems
- EUDAMED SRN
- US-MF-000002128
- Authorised Representative
- Philips Medical Systems Nederland B.V. NL-AR-000001422
Sources (2)
- EUDAMED c88bd5e8-d792-4f26-a9a9-cb24cff54eee 61 fields · synced Jun 18, 2026
- FDA UDI 8c40c1c3-dcc8-4c4e-b083-d024a8de066a 35 fields · synced May 29, 2026