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ORIX Single Lens - Indonesia BPOM Medical Device Registration

ORIX Single Lens is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204220409. The device is manufactured by DANYANG H&C OPTICAL GLASSES CO. LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ATALLA NEW Zealand.

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
ORIX Single Lens
Analysis ID: AKL 11204220409

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. ATALLA NEW Zealand

AR Address

JL.PUTRA I NO.33 A, KAWASAN INDUSTRI PASAR KEMIS

Registration Date

Nov 09, 2022

Expiry Date

Nov 08, 2025

Product Type

Therapeutic Eye Equipment

Prescription show lens.

Non Electromedic Non Sterile

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