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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BEIERSDORF AG.Country of Origin
Germany
Authorized Representative
BEIERSDORF INDONESIAAR 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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