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EXUFIBER AT + - Indonesia BPOM Medical Device Registration

EXUFIBER AT + is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603222575. The device is manufactured by MöLNLYCKE HEALTH CARE AB from Sweden, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MEDI KHARISMA INTERNATIONAL.

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
EXUFIBER AT +

EXUFIBER AG +

Analysis ID: AKL 21603222575

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Sweden

Authorized Representative

PT. MEDI KHARISMA INTERNATIONAL

AR Address

Jl. Darmo kali No.76, RT. 13/RW. 14 Kelurahan Darmo

Registration Date

May 12, 2023

Expiry Date

Aug 15, 2027

Product Type

Surgical Equipment

Hydrophilic wound dressing

Non Electromedic Sterile

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