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WONDFO PRL (CLIA) - Indonesia BPOM Medical Device Registration

WONDFO PRL (CLIA) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101420761. The device is manufactured by SHENZEN TISENC MEDICAL DEVICES CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ZOE PELITA NUSANTARA.

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
WONDFO PRL (CLIA)
Analysis ID: AKL 20101420761

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

ZOE PELITA NUSANTARA

AR Address

JALAN CIKINI II NO 8 B

Registration Date

Apr 22, 2024

Expiry Date

Aug 01, 2028

Product Type

Clinical Chemistry Test System

Prolactin (lactogen) test system (kit & cair)

Invitro Diagnostics

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