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SIMEDICE Intraocluar Lens - Indonesia BPOM Medical Device Registration

SIMEDICE Intraocluar Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31202320177. The device is manufactured by HENAN SIMEDIC BIOTECHNOLOGIES CO.,LTD. from China, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. KATAMATA OPTOMEDIK.

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BPOM Registered
Risk Class Kelas Resiko : D
SIMEDICE Intraocluar Lens
Analysis ID: AKL 31202320177

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

China

Authorized Representative

PT. KATAMATA OPTOMEDIK

AR Address

Komplek Ketapang Indah Blok B2 No.31 Jl. KH. Zainul Arifin Kel.Krukut, Kec.Taman Sari Jakarta Barat

Registration Date

Nov 04, 2023

Expiry Date

Jul 04, 2026

Product Type

Prosthetic Eye Equipment

Intraocular lens.

Non Electromedic Non Sterile

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