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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 32CM Titan15.5F X 32CM T HD CATHETERHD CATHETER (CUFF 27CM FROM TIP)(CUFF 27CM F FDA UDI
Model / Reference
THD155032 FDA UDI
Description
15.5F X 32CM Titan15.5F X 32CM T HD CATHETERHD CATHETER (CUFF 27CM FROM TIP)(CUFF 27CM F FDA UDI

Identifiers

Primary DI / UDI-DI
00884908129328 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 419e072a-1d93-43ac-aa23-008fb4ad907b 34 fields · synced Jun 1, 2026