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AREA - Indonesia BPOM Medical Device Registration

AREA is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20902220613. The device is manufactured by HASELMEIER GMBH from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MERCK CHEMICALS AND LIFE SCIENCES.

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
AREA

ALUETTA

Analysis ID: AKL 20902220613

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

HASELMEIER GMBH

Country of Origin

Germany

Authorized Representative

PT. MERCK CHEMICALS AND LIFE SCIENCES

AR Address

Jl. TB Simatupang No 8 Pasar Rebo, Jakarta

Registration Date

Jun 22, 2022

Expiry Date

Nov 04, 2026

Product Type

Therapeutic General and Individual Hospital Equipment

Piston syringe.

Non Electromedic Non Sterile

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