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RENASYS GO Canister - Indonesia BPOM Medical Device Registration

RENASYS GO Canister is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603026374. The device is manufactured by INTEGRA BIOTECHNICAL S.A.DE C.V (A SUBSIDIARY OF CARLISLE MEDICAL TECHNOLOGIES, LLC) from Mexico, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is BT. Encheval Putera Megatrading.

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
RENASYS GO Canister
Analysis ID: AKL 21603026374

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Mexico

Authorized Representative

BT. Encheval Putera Megatrading

AR Address

JL PULO LENTUT NO. 10 KWS INDUSTRI PULO GADUNG

Registration Date

May 31, 2024

Expiry Date

Dec 31, 2025

Product Type

Surgical Equipment

Surgical instrument motors and accessories/attachments.

Non Electromedic Non Sterile

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