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PRO LM Reusable Video Laryngoscope - Indonesia BPOM Medical Device Registration

PRO LM Reusable Video Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403124720. The device is manufactured by SHENZEN HUGEMED MEDICAL TECHNICAL DEVELOPMENT CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SEKARGUNA MEDIKA.

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
PRO LM Reusable Video Laryngoscope
Analysis ID: AKL 10403124720

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SEKARGUNA MEDIKA

AR Address

JL. Ciputat Raya Nomor 64

Registration Date

Aug 15, 2024

Expiry Date

Jul 05, 2026

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Radiation Electromedics

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