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Ad Rem Technology Sarl
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VEINOPLUS NEUROMUSCULAR STIMULATOR is an FDA 510(k)-cleared medical device (K072252) manufactured by Ad Rem Technology Sarl. This device is classified under the Physical Medicine specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 29, 2008. Regulation: 8.