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INDIBA ACTIV CT 9 - Indonesia BPOM Medical Device Registration

INDIBA ACTIV CT 9 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21403120232. 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 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 ACTIV CT 9
Analysis ID: AKL 21403120232

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

INDIBA S.A

Country of Origin

Spain

Authorized Representative

REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

Nov 18, 2022

Expiry Date

Jul 19, 2027

Product Type

Therapeutic Physical Health Equipment

Ultrasonic diathermy.

Non Radiation Electromedics

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