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CODMAN Bipolar Forceps - Indonesia BPOM Medical Device Registration

CODMAN Bipolar Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603422851. The device is manufactured by GรผNTER BISSINGER MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is TRIDAYA MEDICAL SYNERGY.

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
CODMAN Bipolar Forceps
Analysis ID: AKL 21603422851

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

TRIDAYA MEDICAL SYNERGY

AR Address

Foresta Business Loft 6 Unit 2, Jl. BSD Boulevard Utara, Kelurahan Lengkong Kulon, Kecamatan Pagedangan, Kabupaten Tangerang, Banten 15331, Indonesia

Registration Date

Dec 13, 2024

Expiry Date

Sep 04, 2029

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Electromedic Non Sterile

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