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SIBELMED DATOSPIR AIRA F Spirometer - Indonesia BPOM Medical Device Registration

SIBELMED DATOSPIR AIRA F Spirometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20401023053. The device is manufactured by SIBEL S.A.U from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MEDTEK.

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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Risk Class Kelas Resiko : B
SIBELMED DATOSPIR AIRA F Spirometer
Analysis ID: AKL 20401023053

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SIBEL S.A.U

Country of Origin

Spain

Authorized Representative

MEDTEK

AR Address

Delta Building, Blok A-11, C-1 dan C-2, Jl. Suryopronoto No. 1-9

Registration Date

Sep 16, 2021

Expiry Date

Mar 30, 2026

Product Type

Diagnostic Anesthesia Equipment

Diagnostic spirometer.

Non Radiation Electromedics

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