ISO 14708 Accredited Testing Labs Worldwide
ISO 14708, all parts: Implants for surgery - Active implantable medical devices. Each lab card shows which parts it holds.
- ISO 14708-1Part 1: General requirements for safety, marking and for information to be provided by the manufacturer12 labs →
- ISO 14708-2Part 2: Cardiac pacemakers5 labs →
- ISO 14708-3Part 3: Implantable neurostimulators8 labs →
- ISO 14708-4Part 4: Implantable infusion pump systems7 labs →
- ISO 14708-6Part 6: Particular requirements for active implantable medical devices intended to treat tachyarrhythmia (including implantable defibrillators)2 labs →
- ISO 14708-7Part 7: Particular requirements for cochlear and auditory brainstem implant systems4 labs →
16 accredited laboratories in 6 countries hold ISO 14708 in their ISO/IEC 17025 scope. Primary accreditors include American Association for Laboratory Accreditation, Deutsche Akkreditierungsstelle. In the register, ISO 14708 scope entries most often cover Partikelmessung, Partikeln in Air, Medical equipment, electrical safety and EMC, Water.
Available in 6 Countries
Top matrices for ISO 14708
Top analytes for ISO 14708
- Partikelmessung (1)
- Partikeln (1)
Sample labs
ISO 14708-4 Ed 2.0 (2022-02) – (only Section 27.103 and Section 27.104); ISO 14708-4 Ed 1.0 (2008-11-15) – (only Section 27.103 and Section 27.104); IEC 80601-2-49:2018 Ed.1.0 (Only Section 202.8.102); IEC 61000-4-9 AEI Issued:03/01/20
ISO 14708-1 (2014) clause 27; ISO 14708-3 (2017-04) clause 27; ISO 14708-4 (2008-11-15) clause 27; ISO 14708-4:2022; EN 60945 (2002) [excluding clauses 8 and 11]; IEC 60945 (2002) [excluding clauses 8 and 11]; GR-1089-CORE, Issue 7; I
ISO 14708-1 (2014) clause 27; ISO 14708-3 (2017-04) clause 27; ISO 14708-4 (2008-11-15) clause 27; ISO 14708-4:2022 Clause 27; EN 60945 (2002) [excluding clauses 8 and 11]; IEC 60945 (2002) [excluding clauses 8 and 11]; IEC 61000-6-7
ISO 14708-1 (2014) clause 27; ISO 14708-3 (2017-04) clause 27; ISO 14708-4 (2008-11-15) clause 27; ISO 14708-4:2022 Clause 27; EN 60945 (2002) [excluding clauses 8 and 11]; IEC 60945 (2002) [excluding clauses 8 and 11]; GR-1089-CORE, I
ISO 14708-1(Ed. 2, Ed. 1); ISO 14708-3 (Ed. 2, Ed. 1); ISO 14708-4 (Ed. 1) (All ISO 14708 standards exclude Cl.14.2 and Cl.22); ISO 80601-2-12 (Ed. 1, Ed. 2, Ed. 3); ISO 80601-2-55 (Ed. 1, Ed. 2 + Am 1); ISO 80601-2-56 (Ed. 1, Ed.2 +
ISO 14708-1 : 2014-08 Chirurgische Implantate - Teil 1: Allgemeine Festlegungen für die Sicherheit, Aufschriften und vom Hersteller zur Verfügung zu stellende Informationen ISO 14708-4 : 2008-11⊗ Chirurgische Implantate - Aktive implan
ISO 14708-4 Ed 2.0 (2022-02) – (Only Section 27.103 and Section 27.104); ISO 14708-4 Ed 1.0 (2008-11-15) – (Only Section 27.103 and Section 27.104); IEC 80601-2-49:2018 Ed.1.0 (Only Section 202.8.102); AIM Standard 7351731 Rev. 3.00 20