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CUTEGEL MAX 1400 with Lidocaine - Indonesia BPOM Medical Device Registration

CUTEGEL MAX 1400 with Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602718325. The device is manufactured by BIOTECHNOLOGY NEXT CHALLENGE (BNC) KOREA, INC. from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. HAJU MEDICAL 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
CUTEGEL MAX 1400 with Lidocaine
Analysis ID: AKL 31602718325

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Country of Origin

Korea

Authorized Representative

PT. HAJU MEDICAL INDONESIA

AR Address

Gd. Graha Mampang lt. 2. Jl. Mampang Prapatan Raya no. 100 Duren Tiga Pancoran

Registration Date

May 01, 2021

Expiry Date

Jan 03, 2026

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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