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VIBE P4 - Indonesia BPOM Medical Device Registration

VIBE P4 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20702420015. 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 PT. KIMIA FARMA.

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
VIBE P4
Analysis ID: AKL 20702420015

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SIVANTOS PTE. LTD.

Country of Origin

Singapore

Authorized Representative

PT. KIMIA FARMA

AR Address

Jalan Veteran No.9 RT.00 /RW.00, Desa/Kelurahan Gambir, Kec. Gambir, Kota Adm. Jakarta Pusat, Provinsi DKI Jakarta, Kode Pos: 10110

Registration Date

Feb 02, 2024

Expiry Date

May 31, 2028

Product Type

Prosthetic Ear, Nose and Throat Equipment

Wireless air-conduction hearing aid

Non Radiation Electromedics

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