Medical Device Labelling for Export: UDI, Language and Symbol Requirements
A medical equipment label is a regulated document. It carries the manufacturer’s identity, the device identification, the batch or serial reference, and...
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CE, ISO 13485, FDA, MDR, IEC 60601, RoHS, REACH, UDI, libre vente, Apostille et notification de vigilance pour les équipements médicaux.
A medical equipment label is a regulated document. It carries the manufacturer’s identity, the device identification, the batch or serial reference, and...
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An operating room used to be a set of mechanical systems with a power cable. Today it is a small network: imaging,...
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Patient-contact materials are where medical device compliance gets material-science serious: the foam in an operating table pad, the upholstery on a hospital...
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Unique Device Identification turned the device label into a data carrier. What used to be a model number and a lot code...
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Ask for proof of the label and the manual on a unit, not for a promise that they will be added. Three...
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Medical equipment manufactured in China reaches a hospital’s customs clearance with a paper trail that decides whether it clears in days or...
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Choosing between the FDA’s 510(k) and PMA pathways is the first regulatory decision a medical device seller makes for the US market,...
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Coastal hospitals quietly destroy medical equipment faster than inland facilities: salt-laden humidity attacks castors, bed frames, instrument trays and every fastener on...
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IEC 60601 is the standard family behind nearly every powered device in a hospital room, from ward beds to operating tables to...
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India is among the largest growth markets for imported hospital equipment, and its import pathway runs through CDSCO, the Central Drugs Standard...
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