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ULTRA V HIKO (PCL Ez Cannula) - Indonesia BPOM Medical Device Registration

ULTRA V HIKO (PCL Ez Cannula) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603121652. The device is manufactured by SKINMEDIENCE CO. from Korea, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. REGENESIS 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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Risk Class Kelas Resiko : C
ULTRA V HIKO (PCL Ez Cannula)
Analysis ID: AKL 21603121652

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

SKINMEDIENCE CO.

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jl. Sultan Iskandar Muda No. 7A & B

Registration Date

Mar 25, 2021

Expiry Date

Dec 02, 2025

Product Type

Surgical Equipment

Absorbable polydioxanone surgical suture.

Non Electromedic Sterile

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