Genesis RapidWeld II STW Sterile Tube Welder

FDA UDI

Class II (US FDA UDI)

by Genesisbps Llc

Identity

Trade Name: Genesis RapidWeld II STW Sterile Tube Welder FDA UDI
Generic Name: Laboratory tubing welder FDA UDI
Device Name: The Genesis RapidWeld II STW, model GRW-430-02, is a medical device used in laboratories, designed for the purpose of making sterile connections in PVC tubing in blood processing applications. The device enables fluid transfer while maintaining a closed system without the need for a consumable (disposable wafer). FDA UDI
Model / Reference: GRW-430-02 FDA UDI
Description: The Genesis RapidWeld II STW, model GRW-430-02, is a medical device used in laboratories, designed for the purpose of making sterile connections in PVC tubing in blood processing applications. The device enables fluid transfer while maintaining a closed system without the need for a consumable (disposable wafer). FDA UDI

Identifiers

Catalog Number: 480-RW-2607-02 FDA UDI
Primary DI / UDI-DI: 00866305000264 FDA UDI
FDA Product Code: KSB FDA UDI
GMDN Term: Laboratory tubing welder FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 864.9875 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

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

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Lot / Batch Number

FDA UDI

Serial Number

Yes

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Expiration Date

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Manufacturing Date

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Dimensions & Sizes

Size: Length — 33 Centimeter FDA UDI
Height — 9.9 Centimeter FDA UDI
Width — 14.2 Centimeter FDA UDI
Weight — 2.5 Kilogram FDA UDI

Category: Laboratory tubing welder

Genesis RapidWeld II STW Sterile Tube Welder by Genesisbps Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Genesis RapidWeld STW Sterile Tube Welder — GENESISBPS LLC · 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: Genesisbps Llc

Sources (1)

FDA UDI cf1858e9-2c43-4c09-ab92-8059559806b0 38 fields · synced Jun 8, 2026