PORTEX Reinforced ET Tubes, Single Use - Indonesia BPOM Medical Device Registration

PORTEX Reinforced ET Tubes, Single Use is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403803420. The device is manufactured by SMITHS MEDICAL INTERNATIONAL LIMITED from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. IDS MEDICAL SYSTEMS INDONESIA.

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