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APTOS Light Lift Needle Method S - Indonesia BPOM Medical Device Registration

APTOS Light Lift Needle Method S is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603817792. The device is manufactured by FEUERSTEIN GMBH from Germany, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ETERNAL VAST OCEAN.

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 : C
APTOS Light Lift Needle Method S
Analysis ID: AKL 21603817792

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

FEUERSTEIN GMBH

Country of Origin

Germany

Authorized Representative

ETERNAL VAST OCEAN

AR Address

Jl. Tanah Abang IV No. 34B, RT 004 / RW 03, Gambir, Jakarta Pusat

Registration Date

Dec 22, 2022

Expiry Date

Dec 31, 2024

Product Type

Surgical Equipment

Absorbable poly(glycolide/ l -lactide) surgical suture.

Non Electromedic Sterile

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