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INTEGRA Essential Shunt Kit, Flat Bottom Design - Indonesia BPOM Medical Device Registration

INTEGRA Essential Shunt Kit, Flat Bottom Design is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003615096. The device is manufactured by INTEGRA NEUROSCIENCES PR from Puerto Rico USA, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. VERSACON MEDICAL.

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
INTEGRA Essential Shunt Kit, Flat Bottom Design
Analysis ID: AKL 21003615096

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Puerto Rico USA

Authorized Representative

PT. VERSACON MEDICAL

AR Address

JL ANGGREK NELI MURNI BLOK C NO 30-30 A, PALMERAH

Registration Date

Feb 16, 2021

Expiry Date

Mar 31, 2024

Product Type

Therapeutic Neurology Equipment

Central nervous system fluid shunt and components.

Non Electromedic Sterile

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