KEELER K-LED Portable / Co Axial - Indonesia BPOM Medical Device Registration
KEELER K-LED Portable / Co Axial is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203717395. The device is manufactured by KEELER LIMITED. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. FADZKURUNI.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
KEELER LIMITED.Country of Origin
United Kingdom
Authorized Representative
PT. FADZKURUNIAR Address
SALADDIN SQUARE BLOK B NO.23. JL. MARGONDA RAYA. PANCORAN MAS. KOTA DEPOK
Registration Date
Dec 15, 2021
Expiry Date
Oct 18, 2026
Product Type
Surgical Eye Equipment
Operating headlamp.
Non Radiation Electromedics
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