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ZIMED Intramedullary Nail Systems - Indonesia BPOM Medical Device Registration

ZIMED Intramedullary Nail Systems is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302220449. The device is manufactured by ZIMED MEDIKAL SAN. VE TIC. LTD. STI. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. FIXA MEDIKA TAMA.

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
ZIMED Intramedullary Nail Systems
Analysis ID: AKL 21302220449

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. FIXA MEDIKA TAMA

AR Address

RUKAN ROSES GARDEN 5, BLOK RRG N0. 50, GRAND GALAXY CITY

Registration Date

Nov 17, 2022

Expiry Date

Aug 21, 2027

Product Type

Prosthetic Orthopedic Equipment

Intramedullary fixation rod.

Non Electromedic Sterile

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