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INDIBA ASTER - Indonesia BPOM Medical Device Registration

INDIBA ASTER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403320530. The device is manufactured by INDIBA S.A from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REGENESIS INDONESIA.

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
INDIBA ASTER
Analysis ID: AKL 21403320530

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

INDIBA S.A

Country of Origin

Spain

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

May 08, 2023

Expiry Date

Jan 27, 2027

Product Type

Therapeutic Physical Health Equipment

Shortwave diathermy.

Non Radiation Electromedics

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