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Plus-Sed auto (No Vacuum Plastic Tubes) - Indonesia BPOM Medical Device Registration

Plus-Sed auto (No Vacuum Plastic Tubes) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101220472. The device is manufactured by AQUISEL, S.L. from Spain, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DEMKA SAKTI.

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
Plus-Sed auto (No Vacuum Plastic Tubes)
Analysis ID: AKL 20101220472

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

AQUISEL, S.L.

Country of Origin

Spain

Authorized Representative

PT. DEMKA SAKTI

AR Address

Jl. Tanah Abang III No. 19 A - B, Jakarta Pusat

Registration Date

Apr 11, 2022

Expiry Date

Jun 30, 2026

Product Type

Clinical Chemistry Test System

Blood specimen collection device

Invitro Diagnostics

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