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CloudCath Drain Set - Baxter Configuration

FDA UDI

Class II (US FDA UDI)

by Gastroklenz Inc.

Identity

Trade Name
CloudCath Drain Set - Baxter Configuration FDA UDI
Generic Name
Peritoneal dialysis system FDA UDI
Device Name
Drain Set Finished Sterile, Baxter Compatible FDA UDI
Model / Reference
02PD001 FDA UDI
Description
Drain Set Finished Sterile, Baxter Compatible FDA UDI

Identifiers

Primary DI / UDI-DI
00860006810207 FDA UDI
FDA Product Code
FKX FDA UDI
GMDN Term
Peritoneal dialysis system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.5630 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

Category: Peritoneal dialysis system

CloudCath Drain Set - Baxter Configuration by Gastroklenz Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal dialysis system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gastroklenz Inc.

Sources (1)

  • FDA UDI b09907b3-0919-4ab0-b4a5-be127aa7a869 34 fields · synced Jun 1, 2026