Pure Global

ID-FRESH Sterile Absorbable Viscoelastic Dermal Filler for Tissue Repair - Indonesia BPOM Medical Device Registration

ID-FRESH Sterile Absorbable Viscoelastic Dermal Filler for Tissue Repair is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602918912. The device is manufactured by RUTEC CO., LTD., from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. SOMETECH NEW Zealand.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : D
ID-FRESH Sterile Absorbable Viscoelastic Dermal Filler for Tissue Repair
Analysis ID: AKL 31602918912

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

RUTEC CO., LTD.,

Country of Origin

Korea

Authorized Representative

PT. SOMETECH NEW Zealand

AR Address

AKR Tower Lantai 11 Unit 11G dan 11C, Jalan Panjang Nomor 5 ,RT 011 RW 010, Kec. Kebon Jeruk, Kel. Kebon Jeruk, Jakarta Barat, 11530

Registration Date

Oct 25, 2023

Expiry Date

Aug 16, 2028

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing