0413
INTERTEK SEMKO AB
Designations
Conformity assessment annexesAnnex III, Annex II, Annex V, Annex VI, Annex IV
Designated since2006-04-09
Full scope text from the register
Annexes
- Annex III, Annex II, Annex V, Annex VI, Annex IV
Procedures
- Production quality assurance, EC type-examination, Full quality assurance system, Product quality assurance, EC verification
Products
- Re-usable devices
- Class I devices with a measuring function
- Passive implants
- Electrical devices intended to administer and/or remove medicines or products, body liquids or other substances to or from the body
- Disposables
- Active devices intended for diagnosis
- Active therapeutic devices
- Sterile devices
- Devices with a measuring function
- Wound dressings
- dental devices
- Electrical devices intended for diagnosis
- Devices for the administration to or removal from the patient's body of medicines, body fluids or other substances
- Electrical therapeutic devices
- functional implants
Conformity assessment annexesArticle 8, Article 9
Designated since2006-04-09
Full scope text from the register
Annexes
- Article 8, Article 9
Procedures
- Report consequent on a challenge (Art 8), Opinion on a safeguard action (Art 9)
Products
- Electrical equipment designed for use within certain voltage limits
Source: EU Single Market Compliance Space (SMCS), retrieved 2026-06-23.
https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/free-search?text=0413
https://webgate.ec.europa.eu/single-market-compliance-space/notified-bodies/free-search?text=0413
This page is an informational mirror of the official register. It is not affiliated with the European Commission. Always verify the current designation and scope against the official SMCS record before relying on it.