Identity
- Trade Name
- DDU-1XX Pediatric Rescue Pads FDA UDI
- Generic Name
- External defibrillation electrode, paediatric, single-use FDA UDI
- Model / Reference
- DDP-200P FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00815098020430 FDA UDI
- 510(k) Number
- K033896 FDA UDI
- FDA Product Code
- MKJ FDA UDI
- GMDN Term
- External defibrillation electrode, paediatric, 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
Yes
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
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: External defibrillation electrode, paediatric, single-use
DDU-1XX Pediatric Rescue Pads by Defibtech, L.l.c. — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as External defibrillation electrode, paediatric, single-use.
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- Intellisense™ Pediatric Defibrillation Pads Powerheart® G5 — Cardiac Science Corporation · Class III
- HeartStart Pads — Philips Medical Systems Hsg · Class III
- MedSource Electrodes — MEDSOURCE INTERNATIONAL LLC · Class II
- Powerheart® Pediatric Pads — Zoll Medical Corporation · Class III
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- Cardio Clear — CARDIO MEDICAL PRODUCTS, INC. · Class II
Cleared under the same submission
K033896 also covers:
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
- Defibtech, L.l.c.
Sources (1)
- FDA UDI 19cd812d-4e1b-4276-bc4f-07e65a8b8b00 33 fields · synced May 30, 2026