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C3 Wave System (mrc3rd004)c3 Wave System (mrc3rd004)
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- C3 WAVE SYSTEM (MRC3RD004)C3 WAVE SYSTEM (MRC3RD004) FDA UDI
- Generic Name
- Central venous catheter navigation system, electrocardiographic FDA UDI
- Device Name
- C3 WAVE ECG CABLEC3 WAVE ECG CAB ACCESSORY PACK W/ACCESSORY PACK MAX BARRIER DRAPEMAX BARRIER DRA FDA UDI
- Model / Reference
- MRC3RD004 FDA UDI
- Description
- C3 WAVE ECG CABLEC3 WAVE ECG CAB ACCESSORY PACK W/ACCESSORY PACK MAX BARRIER DRAPEMAX BARRIER DRA FDA UDI
Identifiers
- Catalog Number
- MRC3RD004 FDA UDI
- Primary DI / UDI-DI
- 00884908131529 FDA UDI
- FDA Product Code
- LJS FDA UDI
- GMDN Term
- Central venous catheter navigation system, electrocardiographic FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 880.5970 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
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
Yes
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
C3 Wave System (mrc3rd004)c3 Wave System (mrc3rd004) by Medical Components Inc — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Medical Components Inc
Sources (1)
- FDA UDI 548645fb-9d0e-4115-8ee7-7d81b7dc4216 36 fields · synced May 30, 2026