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XENOLITE-NL Series 800 - Indonesia BPOM Medical Device Registration

XENOLITE-NL Series 800 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11503710743. The device is manufactured by LIFE TECH, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is RAVINDRA PUTRAPRATAMA.

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
XENOLITE-NL Series 800
Analysis ID: AKL 11503710743

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Manufacturer

LIFE TECH, INC.

Country of Origin

United States

Authorized Representative

RAVINDRA PUTRAPRATAMA

AR Address

Pusat Niaga Duta Mas Fatmawati Blok B2-18. Jl. Fatmawati 39 - Cipete Utara Jakarta 12150

Registration Date

May 14, 2020

Expiry Date

Apr 17, 2025

Product Type

Other Radiology Equipment

Personnel protective shield.

Non Electromedic Non Sterile

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