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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 Class Kelas Resiko : A
KEELER K-LED Portable / Co Axial
Analysis ID: AKL 11203717395

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

KEELER LIMITED.

Country of Origin

United Kingdom

Authorized Representative

PT. FADZKURUNI

AR 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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