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Safety Notice for the Frameless SRS QA Target Pointer, Brainlab AG PDF, 83KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - others
Reference 03954/13

Corrective action for TSKgel G8 β-Thal. HSi, Tosoh Bioscience PDF, 133KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 03494/13

Safety Notice for the V60 Ventilator, Respironics California PDF, 170KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03530/13

Safety Notice for Nihon Kohden Telemetry Systems WEP-5204K, WEP-5208K using Software Version ≤ 03-10 PDF, 123KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 04024/13

Lot Recall of the product CELT ACD (6F) Femoral Artery Vascular Closure Device, Vasorum Ltd. PDF, 404KB, File does not meet accessibility standards Date: 22. July 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03705/13

Lot Recall of the CHEX Circular Stapler, Frankenman International Limited PDF, 113KB, File does not meet accessibility standards Date: 22. July 2013 Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 02875/13

Corrective action for Dimension Vista 500® and Dimension® Vista 1500, Siemens PDF, 30KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03107/13

Corrective action for FSH One Step Menopause Test Device (Urine), Innovacon PDF, 416KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03729/13

Recall of the GENESIS II Cruciate Retaining Insert Trials, Smith & Nephew PDF, 53KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 03877/13

Corrective action for IH-1000, Bio-Rad Laboratories PDF, 914KB, File does not meet accessibility standards Date: 18. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 02866/13