MDC

Updated August 13, 2026

MDC is a conformity assessment body based in Germany, identified as notified body NB 0483. NANDO lists it as currently designated under the EU Medical Devices Regulation (MDR) and the In Vitro Diagnostic Medical Devices Regulation (IVDR). Its detailed NANDO scope shows the device categories and conformity assessment activities covered by that designation.

1 Review

5.0 Very good · 1 review

Read all reviews

Overall experience: 5.0

Well-organized / responsive: 4.0

Regulatory pragmatism: 5.0

Technical competence: 4.0

February 28, 2022

Review by company with 10-49 people

QMS audit done

Techdoc audit done

Overall experience
Well-organized / responsive
Regulatory pragmatism
Technical competence

Wait time before QMS audit: 6 Months
Wait time before Techdoc audit: 5 Months
Wait time before QMS certificate: 2 Months
Wait time before Techdoc certificate: ?
Approx. cost (EUR): 30,000 €

Client since 10 years MDR TD and QMS in progress

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Key facts

About MDC

Number: NB 0483
Country: DE
Current designation: MDR and IVDR; View NANDO record; Checked August 13, 2026
Published standard fees: The published MDR and IVDR price lists use activity-specific charges; consult them for current rates and minimum fees.; MDR fee schedule; IVDR fee schedule; Checked August 13, 2026; Standard fees are not a quote. The final cost depends on the device and assessment scope.