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INAMI Universal Trial Frame - Indonesia BPOM Medical Device Registration

INAMI Universal Trial Frame is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201211914. The device is manufactured by INAMI & CO., LTD. from Japan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. EAST RAYA LESTARI.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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BPOM Registered
Risk Class Kelas Resiko : A
INAMI Universal Trial Frame
Analysis ID: AKL 11201211914

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

INAMI & CO., LTD.

Country of Origin

Japan

Authorized Representative

PT. EAST RAYA LESTARI

AR Address

Jalan Rawa kepiting nomor 4 Kawasan Industri Pulo Gadung Jakarta Timur

Registration Date

Feb 08, 2023

Expiry Date

Jan 11, 2028

Product Type

Diagnostic Eye Equipment

Ophthalmic trial lens frame.

Non Electromedic Non Sterile

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