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MC3 Crescent(tm) Jugular Dual Lumen Catheter

FDA UDI

Class II (US FDA UDI)

by Michigan Critical Care Consultants, Inc.

Identity

Trade Name
MC3 Crescent(tm) Jugular Dual Lumen Catheter FDA UDI
Generic Name
Mobile extracorporeal gas exchange system catheter kit FDA UDI
Device Name
Jugular Dual Lumen Catheter 30 Fr FDA UDI
Model / Reference
70130 FDA UDI
Description
Jugular Dual Lumen Catheter 30 Fr FDA UDI

Identifiers

Catalog Number
70130 FDA UDI
Primary DI / UDI-DI
10854916006949 FDA UDI
FDA Product Code
PZS FDA UDI
GMDN Term
Mobile extracorporeal gas exchange system catheter kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.4100 FDA UDI
Commercial Distribution
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

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

Dimensions & Sizes

Size
Catheter Gauge — 30 French FDA UDI

Category: Mobile extracorporeal gas exchange system catheter kit

MC3 Crescent(tm) Jugular Dual Lumen Catheter by Michigan Critical Care Consultants, Inc. — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Mobile extracorporeal gas exchange system catheter kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Michigan Critical Care Consultants, Inc.

Sources (1)

  • FDA UDI 806ff509-190b-4c0a-a8ff-89daa8f7be5e 35 fields · synced Jun 1, 2026