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ONECARE Laryngoscope - Indonesia BPOM Medical Device Registration

ONECARE Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403129227. The device is manufactured by SMEGA TECHNOLOGIES from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. CENTRAL MEDIKA 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 : A
ONECARE Laryngoscope
Analysis ID: AKL 10403129227

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

SMEGA TECHNOLOGIES

Country of Origin

Pakistan

Authorized Representative

PT. CENTRAL MEDIKA INDONESIA

AR Address

Jl. Candi Mutiara Selatan III/ 317 RT.03/06 Kalipancur

Registration Date

Dec 29, 2021

Expiry Date

Dec 28, 2024

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Electromedic Non Sterile

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