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SWANTIA Laryngoscope - Indonesia BPOM Medical Device Registration

SWANTIA Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403420172. The device is manufactured by SWANTIA MEDICAL (PVT) LIMITED from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is TRINITY ALPHA OMEGA.

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 : A
SWANTIA Laryngoscope
Analysis ID: AKL 10403420172

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Pakistan

Authorized Representative

TRINITY ALPHA OMEGA

AR Address

JL. Tanjung Duren Timur V No. 49 Jakarta Barat 11470

Registration Date

Mar 06, 2024

Expiry Date

Dec 05, 2026

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Radiation Electromedics

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