Identity
- Trade Name
- Lrg Switched Int Pdls EUDAMEDHeartStart FDA UDI
- Generic Name
- Internal defibrillation electrode, adult, reusable FDA UDI
- Device Name
- Internal Paddles & Internal Paddle Accs. EUDAMEDLrg Switched Int Pdls FDA UDI
- Model / Reference
- M4742A EUDAMEDLrg Switched Int Pdls FDA UDI
- Description
- Lrg Switched Int Pdls FDA UDI
Identifiers
- Catalog Number
- M4742A FDA UDI
- Primary DI / UDI-DI
- 00884838094734 EUDAMEDFDA UDI
- Basic UDI-DI
- B-00884838094734 EUDAMED
- FDA Product Code
- LDD FDA UDIMKJ FDA UDI
- EMDN Code
- Z12030580 DEFIBRILLATORS - HARDWARE ACCESSORIES EUDAMED
- GMDN Term
- Internal defibrillation electrode, adult, reusable FDA UDI
Classification
- Device Class
- Class IIb EUDAMEDClass II FDA UDI
- Regulation Number
- 870.5300 FDA UDI870.5310 FDA UDI
- Market of Registration
- Austria EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
EUDAMEDFDA UDI
Single Use
No
FDA UDI
Implantable
No
EUDAMEDFDA UDI
Reusable
Yes
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
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Moist Heat or Steam Sterilization FDA UDI
Lrg Switched Int Pdls by Philips Medical Systems — Class IIb — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Authorization Coverage (2 countries)
Regulatory Authorizations
European Union Active
CE/MDD
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-00884838094734 | 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-000002321
- Authorised Representative
- Philips Medizin Systeme Böblingen GmbH DE-AR-000006030
Sources (2)
- EUDAMED 739f322f-16c7-4201-a18d-1b52d65c80df 61 fields · synced Jul 8, 2026
- FDA UDI 2e22d3db-c185-4ca4-9ce2-d67a2fd76241 37 fields · synced May 30, 2026