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Mahurkar

FDA UDI

Class II (US FDA UDI)

by Mozarc Medical US LLC

Identity

Trade Name
MAHURKAR FDA UDI
Generic Name
Triple-lumen haemodialysis catheter FDA UDI
Device Name
Acute Triple Lumen Catheter Kit,Curved Extensions FDA UDI
Model / Reference
8888345637 FDA UDI
Description
Acute Triple Lumen Catheter Kit,Curved Extensions FDA UDI

Identifiers

Primary DI / UDI-DI
10884521006829 FDA UDI
FDA Product Code
NIE FDA UDI
GMDN Term
Triple-lumen haemodialysis catheter 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

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 — 12 French FDA UDI
Length — 24 Centimeter FDA UDI

Category: Triple-lumen haemodialysis catheter

Mahurkar by Mozarc Medical US LLC — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Triple-lumen haemodialysis catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mozarc Medical US LLC

Sources (1)

  • FDA UDI 3c94bd28-25c9-4ae8-a6a4-b3a07c8a5fa5 35 fields · synced Jun 8, 2026