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Medcomp Hemo-Flow Double Lumen Cathetermedcomp Hemo-Flow Double Lumen Catheter

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
MEDCOMP HEMO-FLOW DOUBLE LUMEN CATHETERMEDCOMP HEMO-FLOW DOUBLE LUMEN CATHETER FDA UDI
Generic Name
Double-lumen haemodialysis catheter, implantable FDA UDI
Device Name
15.5F X 24CM HEMO-FLOW®XF DOUBLE LUMEN CATHETER FULLDOUBLE SET (CUFF 19CM FROM TIP)SET (CUF FDA UDI
Model / Reference
DMC641501 FDA UDI
Description
15.5F X 24CM HEMO-FLOW®XF DOUBLE LUMEN CATHETER FULLDOUBLE SET (CUFF 19CM FROM TIP)SET (CUF FDA UDI

Identifiers

Catalog Number
DMC641501 FDA UDI
Primary DI / UDI-DI
00884908140927 FDA UDI
FDA Product Code
MSD FDA UDI
GMDN Term
Double-lumen haemodialysis catheter, implantable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Category: Double-lumen haemodialysis catheter, implantable

Medcomp Hemo-Flow Double Lumen Cathetermedcomp Hemo-Flow Double Lumen Catheter by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Double-lumen haemodialysis catheter, implantable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Medical Components Inc

Sources (1)

  • FDA UDI 7196e900-fdaa-4af0-9b04-997dfc4d8fc0 35 fields · synced Jun 1, 2026