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OPTOP UNIVERSAL TRIAL FRAME - Indonesia BPOM Medical Device Registration

OPTOP UNIVERSAL TRIAL FRAME is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201124879. The device is manufactured by DANYANG XINGDA OPTICAL INSTRUMENT CO. LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SON OF NUSA LOGISTINDO.

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
OPTOP UNIVERSAL TRIAL FRAME
Analysis ID: AKL 11201124879

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

SON OF NUSA LOGISTINDO

AR Address

GREEN LAKE CITY RUKAN CORDOBA BLOK F NO.033

Registration Date

Aug 09, 2021

Expiry Date

May 19, 2026

Product Type

Diagnostic Eye Equipment

Ophthalmic trial lens frame.

Non Electromedic Non Sterile

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