GEISTER Clamp Surgical Instrument (3) - Indonesia BPOM Medical Device Registration
GEISTER Clamp Surgical Instrument (3) is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603520155. The device is manufactured by GEISTER MEDIZINTECHNIK GMBH from Germany, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is MEDTEK.
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.
Risk Classification
Product Class
Kelas : 1
Manufacturer
GEISTER MEDIZINTECHNIK GMBHCountry of Origin
Germany
Authorized Representative
MEDTEKAR Address
DELTA BUILDING BLOK A-11, C-1 & C-2, JL. SURYOPRANOTO NO.1-9, RT/RW 004/007
Registration Date
Jan 17, 2025
Expiry Date
Dec 31, 2026
Product Type
Surgical Equipment
Manual surgical instrument for general use
Non Electromedic Non Sterile
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