“EUROIMMUN” Anti-Glutamate receptor (type NMDA) IIFT - Taiwan Registration 39154efa9e651cd0b163bcd3a02ab2a0

Access comprehensive regulatory information for “EUROIMMUN” Anti-Glutamate receptor (type NMDA) IIFT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 39154efa9e651cd0b163bcd3a02ab2a0 and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE).

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