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INTEGRA Lumbar Drainage Sets - Indonesia BPOM Medical Device Registration

INTEGRA Lumbar Drainage Sets is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21003711252. The device is manufactured by INTEGRA NEUROSCIENCES IMPLANTS (FRANCE) S.A.S. from France, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TRIDAYA 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
INTEGRA Lumbar Drainage Sets
Analysis ID: AKL 21003711252

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

France

Authorized Representative

PT. TRIDAYA MEDICAL SYNERGY

AR Address

Jl. BSD Grand Boulevard, BSD Green Office Park, BSD City, Wing B, 3rd floor, Zone 7C

Registration Date

Apr 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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