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HANSAPLAST Plastic - Indonesia BPOM Medical Device Registration

HANSAPLAST Plastic is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902412539. The device is manufactured by BEIERSDORF MANUFACTURING ARGENTONA S.L from Spain, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is BEIERSDORF INDONESIA.

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 : A
HANSAPLAST Plastic

HANSAPLAST Plastik

Analysis ID: AKL 10902412539

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Spain

Authorized Representative

BEIERSDORF INDONESIA

AR Address

Jl. Raya Randuagung KM. 75. Singosari

Registration Date

Mar 03, 2021

Expiry Date

Dec 13, 2024

Product Type

Therapeutic General and Individual Hospital Equipment

Elastic bandage.

Non Electromedic Non Sterile

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