PRIMAMED SWORD Hartmann Ear Speculum - Indonesia BPOM Medical Device Registration
PRIMAMED SWORD Hartmann Ear Speculum is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703913398. The device is manufactured by A SCHWEICKHARDT GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. DAYA PRIMA MANDIRI JAYA.
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PRIMAMED SCHWERT Hartmann Ear Speculum
Risk Classification
Product Class
Kelas : 1
Manufacturer
A SCHWEICKHARDT GMBH & CO. KG.Country of Origin
Germany
Authorized Representative
PT. DAYA PRIMA MANDIRI JAYAAR Address
JL. KALIGARANG 1A SEMARANG
Registration Date
Nov 30, 2023
Expiry Date
Nov 29, 2026
Product Type
Ear, Nose and Throat Surgical Equipment
Ear, nose, and throat manual surgical instrument.
Non Electromedic Non Sterile
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