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WOWART MONO - Indonesia BPOM Medical Device Registration

WOWART MONO is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603421671. The device is manufactured by DERMALINE CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MITRA HARAPAN MANDIRI.

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 : C
WOWART MONO
Analysis ID: AKL 21603421671

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Korea

Authorized Representative

PT. MITRA HARAPAN MANDIRI

AR Address

The Bellezza Shopping Arcade Lt. 2 SA 69, 70 & 71, Jl. Letjen Soepeno No. 34 Arteri Permata Hijau

Registration Date

Jul 30, 2024

Expiry Date

May 26, 2029

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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