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AyoTes Amphetamine (AMP) Rapid Test (Urine) - Indonesia BPOM Medical Device Registration

AyoTes Amphetamine (AMP) Rapid Test (Urine) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20103320603. The device is manufactured by ASSURE TECH. (HANGZHOU) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. HEALTHY FAMILY FOCUS.

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
AyoTes Amphetamine (AMP) Rapid Test (Urine)
Analysis ID: AKL 20103320603

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. HEALTHY FAMILY FOCUS

AR Address

Komplek Delta Building Blok B 1-2, Jalan Suryopranoto No. 1-9, Prov. DKI Jakarta, Kota Jakarta Pusat, Kec. Gambir, Kel. Petojo Selatan

Registration Date

Nov 13, 2023

Expiry Date

Nov 13, 2026

Product Type

Clinical Toxicology Test System

Amphetamine test system (strip & midstream)

Invitro Diagnostics

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