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GEISTER ValveGate Soft Tissue Protector - Indonesia BPOM Medical Device Registration

GEISTER ValveGate Soft Tissue Protector is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603512151. The device is manufactured by GEISTER MEDIZINTECHNIK GMBH. from Germany, and is classified as Risk Class Kelas Resiko : B. 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.

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BPOM Registered
Risk Class Kelas Resiko : B
GEISTER ValveGate Soft Tissue Protector

GEISTER ValveGate Soft Tissue Protector

Analysis ID: AKL 21603512151

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Germany

Authorized Representative

MEDTEK

AR Address

DELTA BUILDING BLOK A-11, C-1 & C-2, JL. SURYOPRANOTO NO.1-9, RT/RW 004/007

Registration Date

Oct 31, 2024

Expiry Date

Dec 31, 2026

Product Type

Surgical Equipment

Surgical drape and drape accessories.

Non Electromedic Sterile

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