Pro-Fuse®

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name: PRO-FUSE® FDA UDI
Generic Name: Vascular port/catheter FDA UDI
Device Name: 9.6F PLASTIC Pro-Fuse® CT PORT W/ATTACHABLECT PORT W/AT SILICONE CATHETERSILICONE CATHET FDA UDI
Model / Reference: MRPP96AFS FDA UDI
Description: 9.6F PLASTIC Pro-Fuse® CT PORT W/ATTACHABLECT PORT W/AT SILICONE CATHETERSILICONE CATHET FDA UDI

Identifiers

Catalog Number: MRPP96AFS FDA UDI
Primary DI / UDI-DI: 00884908147483 FDA UDI
FDA Product Code: LJT FDA UDI
GMDN Term: Vascular port/catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5965 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

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Vascular port/catheter

Pro-Fuse® by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Vital-Port — COOK INCORPORATED · Class II
Vortex — NAVILYST MEDICAL, INC. · Class II
PowerPort — Bard Access Systems, Inc. · Class II
Deltec — ICU MEDICAL, INC. · Class II

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 36dae05a-b93a-488a-9bdd-8f35c1c024d2 35 fields · synced May 30, 2026