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HANSAPLAST Transparent - Indonesia BPOM Medical Device Registration

HANSAPLAST Transparent is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902412540. 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 PT. 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 Transparent

HANSAPLAST Transparan

Analysis ID: AKL 10902412540

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Spain

Authorized Representative

PT. BEIERSDORF INDONESIA

AR Address

South Quarter Tower C lantai 6 Jl. R.A. Kartini kav.8, Cilandak Barat, Cilandak, Jakarta selatan, DKI Jakarta, 12430

Registration Date

Jul 29, 2024

Expiry Date

Jan 25, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Elastic bandage.

Non Electromedic Non Sterile

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