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MEDEYRA Deep with Lidocaine - Indonesia BPOM Medical Device Registration

MEDEYRA Deep with Lidocaine is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602420168. The device is manufactured by REANZEN CO., LTD from Korea, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. CAWANDRA JAYA 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
MEDEYRA Deep with Lidocaine
Analysis ID: AKL 31602420168

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

REANZEN CO., LTD

Country of Origin

Korea

Authorized Representative

PT. CAWANDRA JAYA INDONESIA

AR Address

Jalan Joe Kelapa Tiga No. 2C RT 001 RW 003

Registration Date

Dec 10, 2024

Expiry Date

Dec 24, 2026

Product Type

Prosthetic Surgical Equipment

Dermal filler

Non Electromedic Sterile

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