WIPAK Steriking Gusseted Rolls - Indonesia BPOM Medical Device Registration
WIPAK Steriking Gusseted Rolls is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20901914419. The device is manufactured by WIPAK LTD. from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. INTERGASTRA NUSANTARA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
WIPAK LTD.Country of Origin
Finland
Authorized Representative
PT. INTERGASTRA NUSANTARAAR Address
Pangeran Jayakarta 24/34-35 Mangga Dua Selatan Sawah Besar- Jakarta Pusat
Registration Date
Mar 29, 2022
Expiry Date
Aug 01, 2025
Product Type
General and Individual Hospital Equipment Monitoring
Sterilization process indicator.
Non Electromedic Non Sterile
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ELMASONIC Med
ELMA SCHMIDBAEUR GMBH.
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