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GPQ PRX T-Lady - Indonesia BPOM Medical Device Registration

GPQ PRX T-Lady is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222676. The device is manufactured by GPQ S.R.L from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REDO MARKETING 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 : B
GPQ PRX T-Lady
Analysis ID: AKL 21603222676

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

GPQ S.R.L

Country of Origin

Italy

Authorized Representative

PT. REDO MARKETING INDONESIA

AR Address

Ruko Renata Jl.Jalur Sutera Timur Blok 1A No. 9 Alam Sutera Kel. Kunciran Kec. Pinang

Registration Date

Nov 10, 2022

Expiry Date

May 05, 2026

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Non Sterile

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