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AGAPPE Qualicheck Norm - Indonesia BPOM Medical Device Registration

AGAPPE Qualicheck Norm is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101810301. The device is manufactured by AGAPPE DIAGNOSTIC SWISTERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is MULTIMEDILAB KARYAMANDIRI.

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
AGAPPE Qualicheck Norm
Analysis ID: AKL 20101810301

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

MULTIMEDILAB KARYAMANDIRI

AR Address

GP plaza lantai 3 unit 6, jalan Gelora II No. 01

Registration Date

May 31, 2022

Expiry Date

Feb 07, 2027

Product Type

Clinical Chemistry Test System

Quality control material (assayed and unassayed) (cair)

Invitro Diagnostics

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