MEDELA Nipple Formers - Indonesia BPOM Medical Device Registration
MEDELA Nipple Formers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902110252. The device is manufactured by MEDELA AG. from Switzerland, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CITRA VITA BUANA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
MEDELA AG.Country of Origin
Switzerland
Authorized Representative
PT. CITRA VITA BUANAAR Address
Jl. M. Hasibuan, Ruko Suncity Square Blok E 18 RT 004 / RW 002
Registration Date
Oct 01, 2024
Expiry Date
Jul 31, 2028
Product Type
Therapeutic General and Individual Hospital Equipment
Nipple shield.
Non Electromedic Non Sterile
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