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VETA Peritoneal Dialysis Catheter

FDA UDI

Class I (US FDA UDI)

by Pfm Medical Incorporated

Identity

Trade Name
VETA Peritoneal Dialysis Catheter FDA UDI
Generic Name
Peritoneal dialysis catheter, acute/chronic FDA UDI
Device Name
VETA Peritoneal Dialysis Stylet FDA UDI
Model / Reference
M8002 FDA UDI
Description
VETA Peritoneal Dialysis Stylet FDA UDI

Identifiers

Catalog Number
M8002 FDA UDI
Primary DI / UDI-DI
00813623040526 FDA UDI
510(k) Number
K113354 FDA UDI
FDA Product Code
GAH FDA UDI
GMDN Term
Peritoneal dialysis catheter, acute/chronic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

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

Category: Peritoneal dialysis catheter, acute/chronic

VETA Peritoneal Dialysis Catheter by Pfm Medical Incorporated — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal dialysis catheter, acute/chronic.

Cleared under the same submission

K113354 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Pfm Medical Incorporated

Sources (1)

  • FDA UDI 54599b93-a89c-48b0-bee9-c95a84039a60 36 fields · synced Jun 1, 2026