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REXTON Arena P 1 - Indonesia BPOM Medical Device Registration

REXTON Arena P 1 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702320140. The device is manufactured by SIVANTOS PTE LTD from Singapore, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is GANTAPI BOJONG ABADI.

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
REXTON Arena P 1
Analysis ID: AKL 20702320140

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SIVANTOS PTE LTD

Country of Origin

Singapore

Authorized Representative

GANTAPI BOJONG ABADI

AR Address

JL. Raya Serpong KM. 8 Blok A No. 1, Komplek Puri Mutiara Serpong

Registration Date

Jun 23, 2023

Expiry Date

Jan 31, 2028

Product Type

Prosthetic Ear, Nose and Throat Equipment

(Deleted) Hearing Aid

Non Radiation Electromedics

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