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ASTERASYS Liftera-A - Indonesia BPOM Medical Device Registration

ASTERASYS Liftera-A is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603324838. The device is manufactured by ASTERASYS CO, LTD from Korea, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. REGENESIS 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 : B
ASTERASYS Liftera-A
Analysis ID: AKL 21603324838

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ASTERASYS CO, LTD

Country of Origin

Korea

Authorized Representative

PT. REGENESIS INDONESIA

AR Address

Jalan Sultan Iskandar Muda No. 7 A dan B, Kebayoran lama Selatan, Kebayoran Lama, Jakarta Selatan

Registration Date

Mar 05, 2024

Expiry Date

Apr 25, 2028

Product Type

Surgical Equipment

Focused ultrasound stimulator system for aesthetic use

Non Radiation Electromedics

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