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KEELER Mini Magnifiers - Indonesia BPOM Medical Device Registration

KEELER Mini Magnifiers is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203128039. 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 FADZKURUNI.

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BPOM Registered
Risk Class Kelas Resiko : A
KEELER Mini Magnifiers

KEELER Mini Loupes

Analysis ID: AKL 11203128039

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

KEELER LIMITED

Country of Origin

United Kingdom

Authorized Representative

FADZKURUNI

AR Address

SALADDIN SQUARE BLOK B NO.23. JL. MARGONDA RAYA. PANCORAN MAS. KOTA DEPOK

Registration Date

Dec 20, 2021

Expiry Date

Oct 18, 2026

Product Type

Surgical Eye Equipment

Ophthalmic operating spectacles (loupes).

Non Electromedic Non Sterile

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