eIFU | vtitan

Instructions for Use

vTitan Corporation provides IFU in electronic form (eIFU) under Regulation (EU) 2021/2226 for healthcare professionals, with a paper version free on request.

Current Instructions for Use Page Updated on: 13-Oct-2026

Check the product name and model number with the package supplied along with the device.

Product Name	Model Number	Basic UDI-DI	IFU Part Number	Revision	Language	Effective Date	Download
Accuflow VE Syringe Pump	VE-002	890614936VE-002C2	981-1009	F	English	28-Aug-2026	PDF

Superseded Revisions

Superseded revisions are no longer current. They are available on request for devices supplied with that revision.

Product Name / Model Number	IFU Part Number	Revision	Valid	Availability
Accuflow VE Syringe Pump / VE-002	981-1009	E	15-May-2026 to 27-Aug-2026	on request - info@vtitan.com
Accuflow VE Syringe Pump / VE-002	981-1009	D	05-Jan-2026 to 14-May-2026	on request - info@vtitan.com
Accuflow VE Syringe Pump / VE-002	981-1009	C	18-Dec-2025 to 04-Jan-2026	on request - info@vtitan.com
Accuflow VE Syringe Pump / VE-002	981-1009	B	28-Nov-2025 to 17-Dec-2025	on request - info@vtitan.com
Accuflow VE Syringe Pump / VE-002	981-1009	A	11-Apr-2025 to 27-Nov-2025	on request - info@vtitan.com

Request a paper copy

A paper copy of any Instructions for Use listed on this page is available free of charge. Quote the device model, IFU part number and revision. Kindly write an email to info@vtitan.com

Report a serious incident

Any serious incident that has occurred in relation to the device should be reported to vTitan and to the competent authority of the Member State in which the user and / or patient is established. Kindly write an email to info@vtitan.com

Manufacturer and EU Authorised Representative

Manufacturer: vTitan Corporation Private Limited,

New Woodlands Building, Estancia IT Park,

Plot No 140, 151, GST Road, Vallancheri Village,

Chengalpattu District, Tamil Nadu – 603202, India

EU REP: Amstermed B.V,
Van der Burchstraat 28,

2132 RN Hoofddorp, Netherlands