Pure Global

AGAPPE SGOT - Indonesia BPOM Medical Device Registration

AGAPPE SGOT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101715968. The device is manufactured by AGAPPE DIAGNOSTIC SWITZERLAND GMBH. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : B
AGAPPE SGOT
Analysis ID: AKL 20101715968

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

PT. MULTIMEDILAB KARYAMANDIRI

AR Address

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

Registration Date

Jun 21, 2022

Expiry Date

Apr 25, 2027

Product Type

Clinical Chemistry Test System

Aspartate amino transferase (AST/SGOT) test system (kit & cair)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from AGAPPE DIAGNOSTIC SWITZERLAND GMBH.
Products from the same manufacturer (3 products)