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Dignity®

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
DIGNITY® FDA UDI
Generic Name
Vascular port/catheter FDA UDI
Device Name
6.6F TITANIUM DIGNITY®MIN PROFILE CT PORT W/PROFILE CT POR PRE-ATTACHED CHRONOFLEX® POLYURETHANE CATHETERPOLYURETHAN FDA UDI
Model / Reference
MRDT66PSN FDA UDI
Description
6.6F TITANIUM DIGNITY®MIN PROFILE CT PORT W/PROFILE CT POR PRE-ATTACHED CHRONOFLEX® POLYURETHANE CATHETERPOLYURETHAN FDA UDI

Identifiers

Catalog Number
MRDT66PSN FDA UDI
Primary DI / UDI-DI
00884908147728 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
Not 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
MRI Safety
MR Conditional FDA UDI

Dignity® 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 8961f478-c717-47ba-8116-3d579e98884f 36 fields · synced Jun 8, 2026