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COAXMED - Indonesia BPOM Medical Device Registration

COAXMED is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603915667. The device is manufactured by BIOTEC ITALIA S.R.L. from Italy, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is HERCA CIPTA DERMAL PERDANA.

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
COAXMED
Analysis ID: AKL 21603915667

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

HERCA CIPTA DERMAL PERDANA

AR Address

Taman Harapan Indah Blok FF 1 B No. 10 Kel. Jelambar Baru, Kec. Grogol Petamburan Jakarta Barat 11460

Registration Date

May 19, 2022

Expiry Date

Mar 22, 2027

Product Type

Surgical Equipment

Contact cooling system for aesthetic use

Non Radiation Electromedics

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