TONTARRA Venous Section Set - Indonesia BPOM Medical Device Registration
TONTARRA Venous Section Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603805060. The device is manufactured by TONTARRA MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEDTEK.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
TONTARRA MEDIZINTECHNIK GMBH.Country of Origin
Germany
Authorized Representative
PT. MEDTEKAR Address
Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9
Registration Date
Sep 29, 2022
Expiry Date
Aug 30, 2027
Product Type
Surgical Equipment
Manual surgical instrument for general use.
Non Electromedic Non Sterile
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