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CEREFORM® SILICONE GEL-FILLED BREAST IMPLANTS - Indonesia BPOM Medical Device Registration

CEREFORM® SILICONE GEL-FILLED BREAST IMPLANTS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31602320230. The device is manufactured by EUROMI BIOSCIENCES from Belgium, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PHARMINDO RHIZOME STURDY.

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
CEREFORM® SILICONE GEL-FILLED BREAST IMPLANTS
Analysis ID: AKL 31602320230

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

EUROMI BIOSCIENCES

Country of Origin

Belgium

Authorized Representative

PHARMINDO RHIZOME STURDY

AR Address

Jalan Arowana No 98 Kel. Kebonagung Kec. Kaliwates

Registration Date

Jul 12, 2023

Expiry Date

Feb 20, 2026

Product Type

Prosthetic Surgical Equipment

Silicone gel-filled breast prosthesis.

Non Electromedic Sterile

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