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PANDA P3 Intraoral Digital Impression Instrument - Indonesia BPOM Medical Device Registration

PANDA P3 Intraoral Digital Impression Instrument is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10605420045. The device is manufactured by ZIYANG FREQTY MEDICAL EQUIPMENT from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is THOMASONG NIRMALA.

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
PANDA P3 Intraoral Digital Impression Instrument
Analysis ID: AKL 10605420045

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

THOMASONG NIRMALA

AR Address

JL. AM SANGAJI NO. 20A KEL. PETOJO UTARA, KEC. GAMBIR JAKARTA TELP. 021-63855888

Registration Date

Jan 25, 2024

Expiry Date

Nov 14, 2026

Product Type

Other Dental Equipment

Dental operative unit and accessories.

Non Radiation Electromedics

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