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BIEN AIR Micro Surgical Drill - Indonesia BPOM Medical Device Registration

BIEN AIR Micro Surgical Drill is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20703513605. The device is manufactured by BIEN AIR SURGERY SA. from Switzerland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is OPMIC PERKASA MANDIRI.

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
BIEN AIR Micro Surgical Drill
Analysis ID: AKL 20703513605

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Switzerland

Authorized Representative

OPMIC PERKASA MANDIRI

AR Address

Jl.Puri Kencana Blok K7-3D 3rd Fl Kembangan Jakarta 11610

Registration Date

Dec 20, 2024

Expiry Date

Dec 31, 2027

Product Type

Ear, Nose and Throat Surgical Equipment

Ear, nose, and throat electric or pneumatic surgical drill.

Non Radiation Electromedics

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