Pure Global

HANSAPLAST Disney - Indonesia BPOM Medical Device Registration

HANSAPLAST Disney is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902811180. 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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : A
HANSAPLAST Disney
Analysis ID: AKL 10902811180

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 30, 2024

Expiry Date

Aug 03, 2028

Product Type

Therapeutic General and Individual Hospital Equipment

Medical adhesive tape and adhesive bandage, non sterile

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing