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ORTHOCEM 1G - Indonesia BPOM Medical Device Registration

ORTHOCEM 1G is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 31302818582. The device is manufactured by TEKNIMED SAS. from France, and is classified as Risk Class Kelas Resiko : D. The authorized representative in Indonesia is PT. FAJAR SELARAS PARTNERS.

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 : D
ORTHOCEM 1G
Analysis ID: AKL 31302818582

Risk Classification

Kelas Resiko : D

Product Class

Kelas : 3

Manufacturer

TEKNIMED SAS.

Country of Origin

France

Authorized Representative

PT. FAJAR SELARAS PARTNERS

AR Address

Komplek Rukan PTC Blok 8C No. 28-29 Pulogadung Tel. 021-46827776 Fax. 021-46827033

Registration Date

Dec 12, 2022

Expiry Date

Sep 14, 2027

Product Type

Prosthetic Orthopedic Equipment

Polymethylmethacrylate (PMMA) bone cement with drug

Non Electromedic Sterile

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