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IMMUCOR Medizinische Diagnostik GmbH

Manufacturer of medical devices registered in the European database in Dreieich, Germany.

Registration number (SRN)	DE-MF-000006494
Role	Manufacturer
Status	Active
Country	Germany
City	63303 Dreieich
Address	Robert-Bosch-Straße, 32 63303 Dreieich
Registered on	2021-06-01

United States market access

FDA establishment register	Not found in the U.S. FDA register

⚠️ Not found is not the same as not registered. The two registers share no common identifier; the comparison is made on company names. This manufacturer may reach the United States through a distributor, or be registered under a name we could not match. State of the FDA register on 2026-08-20.

Notified body certificates

Certificate	Status	Expiry	Type	Body
IX 1191616-9	supplemented	2028-12-03	Technical documentation	NB 0197
IX 1191616-8	supplemented	2028-11-28	Technical documentation	NB 0197
IX 1191616-7	supplemented	2028-10-24	Technical documentation	NB 0197
IX 1191616-6	supplemented	2028-09-27	Technical documentation	NB 0197
IX 1191616-5	supplemented	2028-11-27	Technical documentation	NB 0197
IX 1191616-4	supplemented	2028-12-05	Technical documentation	NB 0197
IX 1191616-3	supplemented	2028-09-27	Technical documentation	NB 0197
IX 1191616-2	supplemented	2028-09-12	Technical documentation	NB 0197
IX 1191616-19	supplemented	2028-11-09	Technical documentation	NB 0197
IX 1191616-18	supplemented	2028-11-09	Technical documentation	NB 0197
IX 1191616-17	supplemented	2028-11-09	Technical documentation	NB 0197
IX 1191616-16	supplemented	2028-10-29	Technical documentation	NB 0197
IX 1191616-15	supplemented	2028-12-05	Technical documentation	NB 0197
IX 1191616-14	supplemented	2028-12-05	Technical documentation	NB 0197
IX 1191616-13	supplemented	2028-11-28	Technical documentation	NB 0197
IX 1191616-12	supplemented	2028-11-21	Technical documentation	NB 0197
IX 1191616-11	supplemented	2028-05-24	Technical documentation	NB 0197
IX 1191616-10	supplemented	2028-12-03	Technical documentation	NB 0197
IX 1191616-1	supplemented	2028-11-21	Technical documentation	NB 0197
HX 1191616-1	supplemented	2028-05-25	Quality management system	NB 0197

⚠️ State of the register on 2026-08-20. EUDAMED shows only the current version of a certificate — earlier versions are not published, by the Commission or by anyone. A certificate shown as valid here may have changed since. For a legally binding check, consult EUDAMED directly.

The SRN is the registration number assigned by the European Commission. It has been mandatory since 28 May 2026 for any operator placing a medical device on the Union market. Contact details are published in the official register; we do not reproduce them here.