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WISAP C3 CERVICAL COLD COAGULATOR - Indonesia BPOM Medical Device Registration

WISAP C3 CERVICAL COLD COAGULATOR is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20801022909. 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 PT. 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 C3 CERVICAL COLD COAGULATOR
Analysis ID: AKL 20801022909

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. BETA MEDICAL

AR Address

Jl. Pangeran Antasari No. 212

Registration Date

Feb 01, 2024

Expiry Date

Jul 26, 2025

Product Type

Diagnostic Gastroenterology-Urology Equipment

Endoscope and accessories.

Non Radiation Electromedics

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