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CALVIAN Bipolar Instrument - Indonesia BPOM Medical Device Registration

CALVIAN Bipolar Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603815856. The device is manufactured by SUTTER MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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 : C
CALVIAN Bipolar Instrument
Analysis ID: AKL 21603815856

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Jul 30, 2021

Expiry Date

Jan 31, 2024

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Electromedic Non Sterile

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