KEELER Fibre Optic Diagnostic Set on Slim Line Handle 2.8V Dry Cell Battery in Case - Indonesia BPOM Medical Device Registration
KEELER Fibre Optic Diagnostic Set on Slim Line Handle 2.8V Dry Cell Battery in Case is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10703914356. The device is manufactured by KEELER LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is EAST RAYA LESTARI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KEELER LTD.Country of Origin
United Kingdom
Authorized Representative
EAST RAYA LESTARIAR Address
Jalan Rawa kepiting nomor 4 Kawasan Industri Pulo Gadung Jakarta Timur
Registration Date
Apr 02, 2020
Expiry Date
Feb 28, 2025
Product Type
Ear, Nose and Throat Surgical Equipment
Otoscope.
Non Radiation Electromedics
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