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DELFIA Xpress PIGF 1-2-3 - Indonesia BPOM Medical Device Registration

DELFIA Xpress PIGF 1-2-3 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101918111. The device is manufactured by WALLAC OY. from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL 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
DELFIA Xpress PIGF 1-2-3
Analysis ID: AKL 20101918111

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

WALLAC OY.

Country of Origin

Finland

Authorized Representative

PT. UBC MEDICAL INDONESIA

AR Address

Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930

Registration Date

Mar 01, 2024

Expiry Date

Oct 22, 2028

Product Type

Clinical Chemistry Test System

Human growth hormone test system (kit & cair)

Invitro Diagnostics

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