Identity
- Trade Name
- PadPro FDA UDI
- Generic Name
- Multifunction cardiac electrode, paediatric FDA UDI
- Model / Reference
- 2602H FDA UDI
Identifiers
- Catalog Number
- 2602H FDA UDI
- Primary DI / UDI-DI
- 10653405077633 FDA UDI
- 510(k) Number
- K002280 FDA UDI
- FDA Product Code
- MKJ FDA UDI
- GMDN Term
- Multifunction cardiac electrode, paediatric FDA UDI
Classification
- Device Class
- Class III FDA UDI
- Regulation Number
- 870.5310 FDA UDI
- Commercial Distribution
- Not 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
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
PadPro by Conmed Corporation — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Conmed Corporation
Sources (1)
- FDA UDI 0d49a3b3-45ac-43e5-8cbd-13f048810a82 37 fields · synced May 31, 2026