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LABAT Audiolite - Indonesia BPOM Medical Device Registration

LABAT Audiolite is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20701220005. The device is manufactured by LABAT ASIA PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. PERMANA PUTRA MANDIRI.

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
LABAT Audiolite
Analysis ID: AKL 20701220005

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

India

Authorized Representative

PT. PERMANA PUTRA MANDIRI

AR Address

Taman Mini Pintu II Atas No.9 Jakarta Timur

Registration Date

Mar 04, 2022

Expiry Date

Jan 17, 2027

Product Type

Diagnostic Ear, Nose and Throat Equipment

Audiometer.

Non Radiation Electromedics

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