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WISAP HD Hysteroscope OPTIC - Indonesia BPOM Medical Device Registration

WISAP HD Hysteroscope OPTIC is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801020225. The device is manufactured by WISAP MEDICAL TECHNOLOGY GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BETA MEDICAL.

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
WISAP HD Hysteroscope OPTIC
Analysis ID: AKL 20801020225

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

BETA MEDICAL

AR Address

Jl. Pangeran Antasari No. 212

Registration Date

Jan 15, 2024

Expiry Date

Jul 26, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories

Non Radiation Electromedics

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