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HANSAPLAST 123 PACK - Indonesia BPOM Medical Device Registration

HANSAPLAST 123 PACK is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603819262. The device is manufactured by BEIERSDORF AG. from Germany, and is classified as Risk Class Kelas Resiko : B. 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 : B
HANSAPLAST 123 PACK
Analysis ID: AKL 21603819262

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

BEIERSDORF AG.

Country of Origin

Germany

Authorized Representative

BEIERSDORF INDONESIA

AR Address

Jl. Raya Randuagung KM. 75. Singosari

Registration Date

May 06, 2021

Expiry Date

Dec 13, 2024

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Non Sterile

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