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GEOMED Retractors - Indonesia BPOM Medical Device Registration

GEOMED Retractors is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21002812179. The device is manufactured by GEOMED MEDIZIN-TECHNIK GMBH & CO. KG. from Germany, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is ARTHA MEDIKA SENTOSA.

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
GEOMED Retractors
Analysis ID: AKL 21002812179

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

ARTHA MEDIKA SENTOSA

AR Address

Ruko Rose Garden 5 Nomor 115, Grand Galaxy City

Registration Date

Apr 08, 2022

Expiry Date

Feb 01, 2027

Product Type

Surgical Neurology Equipment

Self-retaining retractor for neurosurgery.

Non Electromedic Non Sterile

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