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CELETEQUE Dermoscience Restorative Gel - Indonesia BPOM Medical Device Registration

CELETEQUE Dermoscience Restorative Gel is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603520180. The device is manufactured by FIDIA FARMACEUTICI S.P.A from Italy, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PHARMINDO LESTARI AWARD.

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 : B
CELETEQUE Dermoscience Restorative Gel
Analysis ID: AKL 21603520180

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Italy

Authorized Representative

PHARMINDO LESTARI AWARD

AR Address

World Trade Centre (WTC) 1 Building, Floor 15 JI. Jend. Sudirman Kav. 29 - 31, Jakarta 12920, Indonesia

Registration Date

Jan 19, 2025

Expiry Date

Aug 26, 2029

Product Type

Surgical Equipment

Hydrogel wound dressing and burn dressing.

Non Electromedic Non Sterile

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