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CELLONA Synthetic Undercast Padding (Non Sterile) - Indonesia BPOM Medical Device Registration

CELLONA Synthetic Undercast Padding (Non Sterile) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10902123388. The device is manufactured by TWE DIERDORF GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. NUSA ASIA MEDIKA.

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 : A
CELLONA Synthetic Undercast Padding (Non Sterile)
Analysis ID: AKL 10902123388

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Germany

Authorized Representative

PT. NUSA ASIA MEDIKA

AR Address

Rukan CBD, Green Lake City F No. 15 Ketapang. Cipondoh

Registration Date

Jun 10, 2021

Expiry Date

Mar 01, 2025

Product Type

Therapeutic General and Individual Hospital Equipment

Elastic bandage.

Non Electromedic Non Sterile

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