ZIEMER PROCEDURE PACK - Indonesia BPOM Medical Device Registration
ZIEMER PROCEDURE PACK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903022719. The device is manufactured by SIE AG, SURGICAL INSTRUMENT ENGINEERING from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
SIE AG, SURGICAL INSTRUMENT ENGINEERINGCountry of Origin
Switzerland
Authorized Representative
PT. TRIASTRI MEDITAMAAR Address
GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11
Registration Date
May 13, 2020
Expiry Date
Jan 10, 2024
Product Type
General Hospital Equipment and Other Individuals
Vacuum-powered body fluid suction apparatus
Non Electromedic Non Sterile
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