AESCULAP Hernia and Appendix Instruments Set I - Indonesia BPOM Medical Device Registration

AESCULAP Hernia and Appendix Instruments Set I is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603615445. The device is manufactured by AESCULAP AG from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is B. BRAUN MEDICAL INDONESIA.

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