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MI Trial Femoral Head - Indonesia BPOM Medical Device Registration

MI Trial Femoral Head is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302716586. The device is manufactured by SMITH & NEPHEW ORTHOPEDICS (BEIJING) CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. TAWADA HEALTHCARE.

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
MI Trial Femoral Head
Analysis ID: AKL 21302716586

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. TAWADA HEALTHCARE

AR Address

Rukan Permata Senayan Blok A18-19 Lantai 5 Jl. Tentara Pelajar No. 5

Registration Date

Aug 04, 2024

Expiry Date

Dec 31, 2027

Product Type

Prosthetic Orthopedic Equipment

Knee joint patellofemorotibial metal/polymer porous-coated uncemented prosthesis.

Non Electromedic Sterile

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