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C3 Wavec3 Wave

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
C3 WAVEC3 WAVE FDA UDI
Generic Name
Central venous catheter navigation system, electrocardiographic FDA UDI
Device Name
C3 WAVE ECG CABLE & REMOTE COVER ACCESSORY PACKCOVER ACCESS FDA UDI
Model / Reference
MRC3A003 FDA UDI
Description
C3 WAVE ECG CABLE & REMOTE COVER ACCESSORY PACKCOVER ACCESS FDA UDI

Identifiers

Primary DI / UDI-DI
00884908125207 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 Wavec3 Wave 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

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Manufacturer

Sources (1)

  • FDA UDI d5ee47b7-baf7-49bf-8025-8f6488ca8075 35 fields · synced Jun 6, 2026