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SEFFILLER - Indonesia BPOM Medical Device Registration

SEFFILLER is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603127650. The device is manufactured by SEFFILINE S.R.L from Italy, and is classified as Risk Class Kelas Resiko : B. 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 : B
SEFFILLER
Analysis ID: AKL 21603127650

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

SEFFILINE S.R.L

Country of Origin

Italy

Authorized Representative

PHARMINDO RHIZOME STURDY

AR Address

Jalan Arowana No 98 Kel. Kebonagung Kec. Kaliwates

Registration Date

May 10, 2023

Expiry Date

Feb 27, 2026

Product Type

Surgical Equipment

Microneedling Device for Aesthetic Use

Non Electromedic Sterile

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