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SHENDA Laparoscope - Indonesia BPOM Medical Device Registration

SHENDA Laparoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801520021. The device is manufactured by SHENYANG SHENDA ENDOSCOPE CO., LTD from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is EDISON AMBASSADOR MEANS.

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
SHENDA Laparoscope
Analysis ID: AKL 20801520021

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

EDISON AMBASSADOR MEANS

AR Address

Jl. Oasis Sememi Raya No. 1 RT 05 RW 04, Kel. Sememi, Kec. Benowo, Surabaya, Jawa Timur

Registration Date

Jan 15, 2025

Expiry Date

Nov 12, 2029

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Electromedic Sterile

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