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GENBODY Lancing Device - Indonesia BPOM Medical Device Registration

GENBODY Lancing Device is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11603422941. The device is manufactured by CGENIC MEDITECH PVT. LTD. from India, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. GENBODY INDONESIA SEJAHTERA.

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
GENBODY Lancing Device
Analysis ID: AKL 11603422941

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

India

Authorized Representative

PT. GENBODY INDONESIA SEJAHTERA

AR Address

Jl. A. Yani 221-223 Ruko Segitiga Mas Kav. H-6

Registration Date

Dec 22, 2024

Expiry Date

May 09, 2029

Product Type

Surgical Equipment

Manual surgical instrument for general use

Non Electromedic Non Sterile

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