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Low Recirculation Volume Apd Set

FDA UDI

Class II (US FDA UDI)

by Baxter International Inc.

Identity

Trade Name
LOW RECIRCULATION VOLUME APD SET FDA UDI
Generic Name
Peritoneal dialysis system tubing set FDA UDI
Device Name
This automated PD Set is compatible with Baxter Automated PD systems, Baxter PD Transfer Sets and Effluent Sample Bag. Low Recirculation Volume APD set with cassette FDA UDI
Model / Reference
N5C8305C FDA UDI
Description
This automated PD Set is compatible with Baxter Automated PD systems, Baxter PD Transfer Sets and Effluent Sample Bag. Low Recirculation Volume APD set with cassette FDA UDI

Identifiers

Catalog Number
N5C8305C FDA UDI
Primary DI / UDI-DI
00085412087672 FDA UDI
FDA Product Code
FKX FDA UDI
GMDN Term
Peritoneal dialysis system tubing set 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 tubing set

Low Recirculation Volume Apd Set by Baxter International Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Peritoneal dialysis system tubing set.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI e20a5a9b-be6c-4664-9faa-b14ec46ad502 36 fields · synced Jun 1, 2026