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Results for “ANSPACH Dissection Tools”

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Registry EUDAMED 445 FDA 510(k) incl. De Novo 2 FDA PMA GUDID 445

Country / market European Union (all) 445 United States 447

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Belgium 445

Risk class Class I Class IIa 445 Class IIb Class III Class II (US) 2

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Class A Class B Class C Class D IVD General IVD Annex II List A IVD Annex II List B IVD for self-testing Active implantable (AIMDD) Unclassified (FDA) Not classified (FDA)

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447 devices foundsorted by relevance

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ANSPACH Dissection Tools

Synthes GmbH,Switzerland Group of variants

Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMEDGUDID Class:IIa
Anspach Helix Dissection Tools

The Anspach Effort, Inc.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II
Anspach Dissection Tools

The Anspach Effort, Inc.,United States(FDA applicant)

Active Regimes: 510(k) Registry: 510(k) Class:II

Showing 441-447 of 447

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