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ULTRACOL 200 - Indonesia BPOM Medical Device Registration

ULTRACOL 200 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602520012. The device is manufactured by ULTRA V CO., LTD. from Korea, and is classified as Risk Class Kelas Resiko : D. 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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BPOM Registered
Risk Class Kelas Resiko : D
ULTRACOL 200
Analysis ID: AKL 31602520012

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

ULTRA V CO., LTD.

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

Feb 06, 2025

Expiry Date

Dec 05, 2028

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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