RANDOX RX series LDH P-L - Indonesia BPOM Medical Device Registration
RANDOX RX series LDH P-L is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101322664. The device is manufactured by RANDOX LABORATORIES LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. TAMARA OVERSEAS CORPORINDO.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
RANDOX LABORATORIES LTD.Country of Origin
United Kingdom
Authorized Representative
PT. TAMARA OVERSEAS CORPORINDOAR Address
Jl. Pinangsia Timur No. 49 Jakarta 11110
Registration Date
Feb 23, 2023
Expiry Date
Nov 09, 2025
Product Type
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