Intertek

Updated August 13, 2026

Intertek is a conformity assessment body based in Sweden, identified as notified body NB 2862. NANDO lists it as currently designated under the EU Medical Devices Regulation (MDR). Its detailed NANDO scope shows the device categories and conformity assessment activities covered by that designation.

1 Review

3.0 Bad · 1 review

Read all reviews

Overall experience: 3.0

Well-organized / responsive: 4.0

Regulatory pragmatism: 3.0

Technical competence: 4.0

March 30, 2022

Review by company with 1-9 people

QMS audit done

Techdoc audit done

Overall experience
Well-organized / responsive
Regulatory pragmatism
Technical competence

Wait time before QMS audit: ?
Wait time before Techdoc audit: 6 Months
Wait time before QMS certificate: ?
Wait time before Techdoc certificate: ?
Approx. cost (EUR): Not specified

Related resources

No image yet.

Notified body

DQS

2 reviews · updated about 3 hours ago

No image yet.

Notified body

MDC

1 review · updated about 3 hours ago

No image yet.

Notified body

Tüv Nord (Poland)

1 review · updated about 3 hours ago

Key facts

About Intertek

Number: NB 2862
Country: SE
Current designation: MDR; View NANDO record; Checked August 13, 2026
Published standard fees: Published standard fees include SEK 41,000 per audit day and SEK 5,500 per hour for clinical expert assessment.; MDR fee schedule; Checked August 13, 2026; Standard fees are not a quote. The final cost depends on the device and assessment scope.