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DEXELL SHOOT - Indonesia BPOM Medical Device Registration

DEXELL SHOOT is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20903023183. The device is manufactured by ISTEM MEDIKAL MEDIKAL DEVICE AND INDUSTRY LTD. STI. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. JAYA ABADI 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 : B
DEXELL SHOOT

DEXELL VUR

Analysis ID: AKL 20903023183

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. JAYA ABADI MEDIKA

AR Address

Wisma Ritra Lt 2, Jl.Buncit Raya No. 6 Kalibata

Registration Date

Jun 10, 2020

Expiry Date

Dec 31, 2024

Product Type

General Hospital Equipment and Other Individuals

Patient lubricant.

Non Electromedic Sterile

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