Nipro Set Blood Tubing Set With Transducer Protectors And Priming Set

FDA UDI

Class II (US FDA UDI)

by Nipro Medical Corporation

Identity

Trade Name: NIPRO SET BLOOD TUBING SET WITH TRANSDUCER PROTECTORS AND PRIMING SET FDA UDI
Generic Name: Haemodialysis blood tubing set, single-use FDA UDI
Device Name: PUMP SEGMENT 8.0mm PRIMING VOLUME 149 ML EQUIPMENT FRESENIUS 2008 FDA UDI
Model / Reference: A209Y/V803 FDA UDI
Description: PUMP SEGMENT 8.0mm PRIMING VOLUME 149 ML EQUIPMENT FRESENIUS 2008 FDA UDI

Identifiers

Catalog Number: BL+A209Y/V803 FDA UDI
Primary DI / UDI-DI: 00383790004053 FDA UDI
FDA Product Code: FJK FDA UDI
GMDN Term: Haemodialysis blood tubing set, single-use FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 876.5820 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Haemodialysis blood tubing set, single-use

Nipro Set Blood Tubing Set With Transducer Protectors And Priming Set by Nipro Medical Corporation — Class II — FDA UDI — listed in FDA GUDID

Similar devices

Also classified as Haemodialysis blood tubing set, single-use.

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CombiSet — Fresenius Medical Care Holdings, Inc. · Class II
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SAMI Hemofiltration Cassette — Dialco Medical Inc · Class II
5008X — Fresenius Medical Care Renal Therapies Group, LLC · Class II
Molded Products, Inc. — MOLDED PRODUCTS INC. · Class II
Lifemed Low Volume Tubing Set — Lifemed of California · Class II
CombiSet — Fresenius Medical Care Holdings, Inc. · Class II

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Nipro Medical Corporation

Sources (1)

FDA UDI 57731b13-ecb4-4bf1-9c3d-b9767327ea2d 34 fields · synced Jun 8, 2026