VACUETTE Tourniquet - Indonesia BPOM Medical Device Registration
VACUETTE Tourniquet is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11604912767. The device is manufactured by KIMETEC GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SABA INDOMEDIKA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KIMETEC GMBHCountry of Origin
Germany
Authorized Representative
PT. SABA INDOMEDIKAAR Address
Ruko Kedoya Elok Plaza DB-33 Jl. Panjang No.7-9
Registration Date
Jul 02, 2024
Expiry Date
Jul 02, 2026
Product Type
Therapeutic Surgical Equipment
Nonpneumatic tourniquet.
Non Electromedic Non Sterile
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