Diapact®

FDA UDI

Class II (US FDA UDI)

by B. Braun Medical Inc.

Identity

Trade Name: Diapact® FDA UDI
Generic Name: Haemodialysis blood tubing set, single-use FDA UDI
Device Name: Drain Bags FDA UDI
Model / Reference: 7210511 FDA UDI
Description: Drain Bags FDA UDI

Identifiers

Catalog Number: 7210511 FDA UDI
Primary DI / UDI-DI: 04039239047131 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

Diapact® by B. Braun Medical Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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

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NIPRO SET BLOOD TUBING SET WITH TRANSDUCER PROTECTORS AND PRIMING SET — NIPRO MEDICAL CORPORATION · Class II
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Molded Products, Inc. — MOLDED PRODUCTS INC. · Class II
Lifemed Low Volume Tubing Set — Lifemed of California · 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: B. Braun Medical Inc.

Sources (1)

FDA UDI 56f31bca-f48a-4325-b637-978c2ca94a51 37 fields · synced May 30, 2026