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RIESTER Ri-Standard Laryngoscope - Indonesia BPOM Medical Device Registration

RIESTER Ri-Standard Laryngoscope is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403513133. The device is manufactured by MEDICAL DEVICE (PVT) LTD. from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. LABORA MANDIRI INDO PRATAMA.

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
RIESTER Ri-Standard Laryngoscope
Analysis ID: AKL 10403513133

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Pakistan

Authorized Representative

PT. LABORA MANDIRI INDO PRATAMA

AR Address

Jl. C. Simanjuntak No. 47

Registration Date

May 21, 2021

Expiry Date

Jun 16, 2025

Product Type

Therapeutic Anesthesia Equipment

Rigid laryngoscope.

Non Radiation Electromedics

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