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GOBBLE Percussion Reflex Hammer - Indonesia BPOM Medical Device Registration

GOBBLE Percussion Reflex Hammer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11001126639. The device is manufactured by GOBBLE SURGICAL INC. from Pakistan, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PUTRASEJATI BUSINESS SUCCESS.

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
GOBBLE Percussion Reflex Hammer
Analysis ID: AKL 11001126639

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Pakistan

Authorized Representative

PUTRASEJATI BUSINESS SUCCESS

AR Address

Rukan Crown Blok A No.35 Green Lake City, Kel.Petir Kec.Cipondoh, Kota Tangerang 15147

Registration Date

Nov 06, 2021

Expiry Date

Jul 18, 2024

Product Type

Diagnostic Neurology Equipment

Percussor.

Non Electromedic Non Sterile

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