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CODMAN Disposable Perforator - Indonesia BPOM Medical Device Registration

CODMAN Disposable Perforator is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002420059. The device is manufactured by INTEGRA LIFESCIENCES PRODUCTION CORPORATION from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is 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 : B
CODMAN Disposable Perforator
Analysis ID: AKL 21002420059

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

United States

Authorized Representative

TRIDAYA MEDICAL SYNERGY

AR Address

Foresta Business Loft 6 Unit 2 BSD City, Jl. BSD Boulevard Utara, Kode Pos 15331

Registration Date

Jul 08, 2024

Expiry Date

Feb 13, 2029

Product Type

Surgical Neurology Equipment

Manual cranial drills, burrs, trephines, and their accessories

Non Electromedic Sterile

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