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OPTOP Trial Lens Set - Indonesia BPOM Medical Device Registration

OPTOP Trial Lens Set is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11201124495. 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 PT. 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 Trial Lens Set
Analysis ID: AKL 11201124495

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SON OF NUSA LOGISTINDO

AR Address

GREEN LAKE CITY RUKAN CORDOBA BLOK F NO.033

Registration Date

Jul 26, 2021

Expiry Date

May 19, 2026

Product Type

Diagnostic Eye Equipment

Ophthalmic trial lens set.

Non Electromedic Non Sterile

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