Span-America Medical Systems, Inc.

• Ministero della salute - Direzione generale dei dispositivi medici e del servizio farmaceutico
  ItalyContact the authority →

No certificates registered for this manufacturer.

Devices placed in 4 countries

• Norway354
• Ireland43
• Denmark18
• XI2

4 contacts identified

• LT
  LOGAR Taydis

  PRRC
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• RE
  RAMSBOTTOM Erika

  PRRC
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• LOGAR Taydis
  1. The technical documentation and the EU declaration of conformity are drawn up and kept up-to-date 2. The post-market surveillance obligations are complied with in accordance with Article 10(10)/Article 83.
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• RAMSBOTTOM Erika
  1. The conformity of the devices is appropriately checked, in accordance with the quality management system under which the devices are manufactured, before a device is released. 2. The post-market surveillance obligations are complied with in accordance with Article 10(10). 3. The reporting obligations referred to in Articles 87 to 91 (Vigilance) are fulfilled. 4. In the case of investigational devices, the statement referred to in Section 4.1 of Chapter II of Annex XV is issued.
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• Advena SRL — represents — Span-America Medical Systems, Inc.
• Advena Limited — represents — Span-America Medical Systems, Inc.
• LOGAR Taydis — Span-America Medical Systems, Inc.
• RAMSBOTTOM Erika — Span-America Medical Systems, Inc.