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SERENITY PULMO-6 COPD Screener - Indonesia BPOM Medical Device Registration

SERENITY PULMO-6 COPD Screener is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401411154. The device is manufactured by VITALOGRAPH LTD. from Ireland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SERENITY 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
SERENITY PULMO-6 COPD Screener
Analysis ID: AKL 20401411154

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

VITALOGRAPH LTD.

Country of Origin

Ireland

Authorized Representative

PT. SERENITY INDONESIA

AR Address

Komp. Ruko Griya Inti Sentosa Jl. Griya Agung Blok O No. 96 Sunter

Registration Date

Mar 14, 2019

Expiry Date

Mar 11, 2024

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

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