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GEA Lancing Device - Indonesia BPOM Medical Device Registration

GEA Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603902479. The device is manufactured by HUAIAN TIANDA MEDICAL INTERUMENTS CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. MEGA PRATAMA MEDICALINDO.

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
GEA Lancing Device
Analysis ID: AKL 11603902479

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. MEGA PRATAMA MEDICALINDO

AR Address

Jl. Pluit Raya 133 Blok A.3

Registration Date

Aug 05, 2022

Expiry Date

Aug 04, 2025

Product Type

Surgical Equipment

Manual surgical instrument for general use.

Non Electromedic Non Sterile

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