AESCULAP Genito Urinary Instrument - Indonesia BPOM Medical Device Registration
AESCULAP Genito Urinary Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10804808558. 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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Risk Classification
Product Class
Kelas : 1
Manufacturer
AESCULAP AG.Country of Origin
Germany
Authorized Representative
B. BRAUN MEDICAL INDONESIAAR Address
Gedung Tempo Scan Tower Lantai 30, Jl. HR Rasuna Said Kav. 3-4 RT 009 RW 004 Kel. Kuningan Timur, Kec. Setiabudi, Kota Administrasi Jakarta Selatan
Registration Date
Oct 06, 2022
Expiry Date
Nov 18, 2026
Product Type
Gastroenterology-Surgical Urology Equipment
Manual gastroenterology-urology surgical instrument and accessories.
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