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Specialist in aids for tracheostomy care: development, distribution and care in tracheotomy, laryngectomy and ventilation

FA

Andreas Fahl Medizintechnik-Vertrieb GmbH

Cologne · Berlin · Wiener Neudorf · GlattbruggNew on Amplifa

1992Founded
300Employees
4Sites in DACH
around 4,000Products in the portfolio
82+Countries of delivery

About FAHL

Since 1992, Andreas Fahl Medizintechnik-Vertrieb GmbH has specialised in the care of tracheotomised and laryngectomised patients as well as long-term ventilated patients. The portfolio comprises around 4,000 medical devices such as tracheostomy tubes, speaking valves, tracheostomy valves, artificial noses (HME), products for secretion management, ventilation, cleaning and care as well as paediatric care – partly in-house developments, partly complementary trade products. In-house developments and manufactured products are produced predominantly through cooperations with German production sites; customised adaptations of tracheostomy tubes are carried out in the company's own workshop. The headquarters is located in Cologne, with further sites in Berlin, Wiener Neudorf (Austria) and Glattbrugg (Switzerland). Around 300 employees supply hospitals, care facilities, specialised trade and patients; in total, more than 150,000 patients in over 80 countries have been supplied. In addition to distribution, the company offers discharge management, speech therapy, seminars and a 24-h emergency service for technical aids.

Site
Cologne
Processes
Development and manufacture of medical devices (tracheostomy aids), Customised adaptation of tracheostomy tubes in the in-house workshop, Cooperation with production sites in Germany ('Made in Germany'), 24-h emergency service for technical aids (ventilation and oxygen devices, suction devices), 24-h emergency service (technical aids), Discharge/care management, Speech therapy, Seminars and workshops
Materials
Medical devices (tracheostomy aids)
Certificates
EN ISO 13485, MDR Annex IX, MDR Annex IX (NB 0482)
Founded
1992
Employees
300
Industries
Homecare, Intensive care medicine, Hospitals, Care facilities, Specialised trade, Rehab/persistent vegetative state
  1. 01

    Product development with user feedback

  2. 02

  3. 03

    Quality management (EN ISO 13485)

  4. 04

    Distribution to hospitals, specialised trade and homecare

  5. 05

    Logistics and delivery

  6. 06

    Consulting, instruction and service (discharge management, speech therapy, 24-h

Products and Manufacturing

MD

Medical devices (tracheostomy aids)

Non-active, non-implantable products for anaesthesia, emergency and intensive care, predominantly made of plastic.

Sites

Cologne

DE

Headquarters, central organisation of care

  • In-house workshop for customised adaptations

Berlin

DE

Branch office

Wiener Neudorf

AT

Subsidiary Austria

Glattbrugg

CH

Subsidiary Switzerland

Industries

HomecareIntensive care medicineHospitalsCare facilitiesSpecialised tradeRehab/persistent vegetative stateENT

Processes & technical limits

ProcessesToleranceMax. partWeightLot sizeMaterials
Development and manufacture of medical devices (tracheostomy aids)Assembly–––––
Customised adaptation of tracheostomy tubes in the in-house workshopAssembly–––––
Cooperation with production sites in Germany ('Made in Germany')Assembly–––––
Assembly–––––
24-h emergency service for technical aids (ventilation and oxygen devices, suction devices)Assembly–––––

Additional services

24-h emergency service (technical aids)Discharge/care managementSpeech therapySeminars and workshopsProduct and topic trainingHandling of formalities for medical aid reimbursementin-house development and manufacturing (Made in Germany)customised productions (in-house workshop)delivery/logisticsexport/global business with distributor supportproduct registration support

Reference customers

Purchasing associations, hospital groups and logistics providers (partner supplier)Distribution of BLOM-SINGER® products

Quality

Quality assurance is carried out in accordance with EN ISO 13485; CE marking of the products is certified in accordance with MDR Annex IX by the Notified Body DNV Medcert GmbH (NB 0482). A compliance and CAPA reporting system complements the quality management.

EvidenceCologne
EN ISO 13485
MDR Annex IX (NB 0482)

History

  1. 1992

    Founded as a sole proprietorship in a small office in Cologne

  2. 2002

    Opening of the Berlin branch office

  3. 2003

    Establishment of the Austrian subsidiary

  4. 2019

    Establishment of the Swiss subsidiary

  5. 2025

    Integration of Orbisana Healthcare GmbH into the Fahl Group; around 300 employees worldwide

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