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Split-Cath®iii

FDA UDI

Class II (US FDA UDI)

by Medical Components Inc

Identity

Trade Name
SPLIT-CATH®III FDA UDI
Generic Name
Double-lumen haemodialysis catheter, implantable FDA UDI
Device Name
14F X 32CM SPLIT CATH®III CATHETER SETCATHETER SET (CUFF 27CM FROM TIP)(CUFF 27CM F FDA UDI
Model / Reference
DASPC32-3 FDA UDI
Description
14F X 32CM SPLIT CATH®III CATHETER SETCATHETER SET (CUFF 27CM FROM TIP)(CUFF 27CM F FDA UDI

Identifiers

Catalog Number
DASPC32-3 FDA UDI
Primary DI / UDI-DI
00884908141726 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

Split-Cath®iii by Medical Components Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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 6f0bd73d-59be-4afa-b474-397ab57a4f6a 35 fields · synced May 31, 2026