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Apheresis devices

Apheresis therapy devices

EMDN code B0302

21 manufacturers, 166 models including 166 on the market, 12 countries

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Manufacturers registered in Europe (EUDAMED) 21
  • On the market
  • No longer marketed
  • 93/42 Former directive, not yet certified under the MDR
  • Click a manufacturer to see its full range, a model to open its EUDAMED record.
ManufacturerCountryRegistered modelsClassContact
Kaizenendustri Türkiye
99 others
IIb 93/42 Website info@kaizenendustri.com EUDAMED record Report an error
Sb-Kawasumi Laboratories FDA EU representative : Medical Technology Promedt Consulting GmbH (Germany) Japan
9 others
IIb MDR, 93/42 MDR@sb-kawasumi.jp EUDAMED record Report an error
Infomed FDA EU representative : INFOMED SAS (France) Switzerland
6 others
IIa MDR, 93/42 Website regulatory@infomed.biz EUDAMED record Report an error
Asahi Kasei Medical FDA EU representative : Asahi Kasei Medical Europe GmbH (Germany) Japan
1 other
IIb MDR EUDAMED record Report an error
Bbraun FDA Germany, Italy IIa, IIb, III MDR Website eudamed@bbraun.com EUDAMED record Report an error
Glycorex Sweden IIb 93/42 Website EUDAMED record Report an error
Medica Italy IIb MDR Website EUDAMED record Report an error
Meise Germany IIa MDR mail@meise.com EUDAMED record Report an error
Maco Pharma FDA France IIa, IIb 93/42 eudamed@macopharma.com EUDAMED record Report an error
MTP Medical Technologies Germany IIa MDR Website info@mtp-pirna.de EUDAMED record Report an error
Shandong Zhongbaokang Medical Implements EU representative : Shanghai International Holding Corp. GmbH(Europe) (Germany) China IIb MDR EUDAMED record Report an error
Delta Med FDA Italy IIa MDR info@numantec.eu EUDAMED record Report an error
Jafron EU representative : Shanghai International Holding Corp. GmbH(Europe) (Germany) China IIa MDR EUDAMED record Report an error
Jimro EU representative : Emergo Europe B.V. (Netherlands) Japan IIb MDR Website EUDAMED record Report an error
Kaneka FDA EU representative : Kaneka Medical Europe N.V. (Belgium) Japan IIb 93/42 Website EUDAMED record Report an error
Plas-Free EU representative : MedNet EC-REP IIb GmbH (Germany) Israel IIb MDR Website EUDAMED record Report an error
Tequir Spain IIb MDR Website EUDAMED record Report an error
Therakos FDA Ireland IIa MDR Website regulatory@therakos.com EUDAMED record Report an error
Thermogenesis FDA EU representative : MDSS GmbH (Germany) United States IIa MDR Website regulatoryaffairs@thermogenesis.com EUDAMED record Report an error
Vantive FDA EU representative : Vantive S.r.l. (Italy) Switzerland IIa MDR Website EUDAMED record Report an error
Zhengyuan Technology EU representative : Scinomed Deutschland GmbH (Germany) China IIb 93/42 EUDAMED record Report an error

A model registered in EUDAMED is not necessarily sold in your country. Check availability and CE marking with the manufacturer.

Other manufacturers known in the United States (FDA) 2

Manufacturers selling this type of device in the United States according to the FDA, not yet in EUDAMED for this category. Some do sell in Europe: registration of devices already on the market is mandatory until 28 November 2026, and some are registered under their parent company’s name. The category is inferred automatically from the US classification and may include related products.

ManufacturerCountryBrandsFDA clearance
HARMAC MEDICAL PRODUCTS, INC. United States – registered
MACK MOLDING COMPANY United States – registered

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