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BISSINGER Electrosurgical Instrument - Indonesia BPOM Medical Device Registration

BISSINGER Electrosurgical Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20804320322. The device is manufactured by GUNTER BISSINGER MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. 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 : C
BISSINGER Electrosurgical Instrument
Analysis ID: AKL 20804320322

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

PT. SOMETECH NEW Zealand

AR Address

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

Registration Date

Sep 02, 2023

Expiry Date

Apr 18, 2028

Product Type

Gastroenterology-Surgical Urology Equipment

Endoscopic electrosurgical unit and accessories.

Non Electromedic Non Sterile

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