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Impressum

SFM Hospital Products GmbH
 
Registred office:
Segelfliegerdamm 67-89
D-12487 Berlin (Germany)
 
Postal address:
Alexander-Meissner-Strasse 14
D-12526 Berlin (Germany)
 
Tel: +49 (0) 30 639 788 25
Fax: +49 (0) 30 639 085 19
eMail: info@sfm-berlin.de
HP: www.sfm-berlin.de
 
Managing Director:
Dipl.-Ing. Vera Lindner
 
Competent Court Berlin-Charlottenburg, Commercial Register no. HRB 64980 B
TAX Number: 37/501/20430
Turnover Tax no. :  DE 812329339
 
 
 

About us

We at SFM Hospital Products GmbH would like to thank you for your interest in our product range, which covers the following items:

    • Infusion sets
    • Blood transfusion sets
    • Disposable syringes with needles
    • Examination gloves
    • Surgical gloves
    • Hypodermic needles
    • Plaster
    • X-ray Chemicals

SFM Hospital Products GmbH was founded on 25 September 1997 and is an independent service enterprise operating in the area of medical engineering and technology.

The main focus of our enterprise is retail trade in medical consumables. In the last years, the firm SFM can look back on an annual big sales increase as well as on a constantly increasing number of satisfied customers, mainly in Russia and other GUS countries.

The philosophy of our enterprise is to help our partner find the optimal way of efficiently transposing their interests into actions.

Quality, swift problem-solving and hence customer satisfaction has always been a top priority for us - and our ISO 9001:2000 certification is testimony to our commitments. We are therefore not only interested in sales but also place importance on the following services:

    • Analysis and implementation of customer-specific product requirements
    • Reliable conclusion of contracts
    • Insurance cover for transportation of goods
    • On-schedule delivery of goods to customer

SATISFIED CUSTOMERS - THE BEST REWARD FOR OUR WORK

All the products in our range comply with both the relevant requirements of the German Medical Devices Act (MPG) and the European Council Directive 93/42/EEC, modified by directive 2007/47/EG, on Medical Devices with regard to the CE marking. Compliance with these regulations is monitored by DEKRA Intertek Certification GmbH. The implementation of a quality management system in accordance with DIN EN ISO 9001:2008 and EN ISO 13485:2010 ensures that high quality prevails not only in our products but also in our order processing procedures.