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ENDO Knee System : Tibial - Indonesia BPOM Medical Device Registration

ENDO Knee System : Tibial is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21302420335. The device is manufactured by BEIJING CHUNLIZENGDA MEDICAL INSTRUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. ENDO INDONESIA.

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
ENDO Knee System : Tibial
Analysis ID: AKL 21302420335

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. ENDO INDONESIA

AR Address

Jl. Raya Menganti 14

Registration Date

Sep 09, 2024

Expiry Date

Sep 09, 2027

Product Type

Prosthetic Orthopedic Equipment

Knee joint patellofemorotibial polymer/metal/polymer semi-constrained cemented prosthesis.

Non Electromedic Sterile

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