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ELLIQUENCE Surgi-Max Ultra - Indonesia BPOM Medical Device Registration

ELLIQUENCE Surgi-Max Ultra is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520076. The device is manufactured by ELLIQUENCE, LLC from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. MAIN MEDICAL SYNERGY.

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
ELLIQUENCE Surgi-Max Ultra
Analysis ID: AKL 21603520076

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

ELLIQUENCE, LLC

Country of Origin

United States

Authorized Representative

PT. MAIN MEDICAL SYNERGY

AR Address

Jalan Gajah Mada No. 112 G-H

Registration Date

Feb 10, 2025

Expiry Date

Feb 12, 2029

Product Type

Surgical Equipment

Electrosurgical cutting and coagulation device and accessories.

Non Radiation Electromedics

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