EURONDA E9 Inspection Med B-Type Autoclave - Indonesia BPOM Medical Device Registration
EURONDA E9 Inspection Med B-Type Autoclave is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903510138. The device is manufactured by EURONDA SPA. from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is CITRA VITA BUANA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
EURONDA SPA.Country of Origin
Italy
Authorized Representative
CITRA VITA BUANAAR Address
Jl. M. Hasibuan, Ruko Suncity Square Blok E-18 RT 004 RW 002
Registration Date
Jul 22, 2022
Expiry Date
Dec 31, 2027
Product Type
General Hospital Equipment and Other Individuals
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