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STI Sinuscope - Indonesia BPOM Medical Device Registration

STI Sinuscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703127026. The device is manufactured by TIANJIN BOLANG SCIENCE-TECHNOLOGY DEVELOPMENT CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is SOMETECH 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 : B
STI Sinuscope
Analysis ID: AKL 20703127026

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G, Jl. Panjang No. 5

Registration Date

Nov 16, 2021

Expiry Date

Aug 31, 2026

Product Type

Ear, Nose and Throat Surgical Equipment

Nasopharyngoscope (flexible or rigid) and accessories.

Non Electromedic Non Sterile

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