Pure Global

NAVITAE - Indonesia BPOM Medical Device Registration

NAVITAE is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21204813544. The device is manufactured by NOVAX PHARMA SARL. from Monaco, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is ENSEVAL PUTERA MEGATRADING TBK.

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.

Free Database
Powered by Pure Global AI
BPOM Registered
Risk Class Kelas Resiko : C
NAVITAE
Analysis ID: AKL 21204813544

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Manufacturer

NOVAX PHARMA SARL.

Country of Origin

Monaco

Authorized Representative

ENSEVAL PUTERA MEGATRADING TBK

AR Address

Jalan Pulo Lentut No.10 Kawasan Industri Pulogadung, Jakarta Timur

Registration Date

Aug 23, 2022

Expiry Date

Jun 02, 2027

Product Type

Therapeutic Eye Equipment

Soft (hydrophilic) contact lens care products.

Non Electromedic Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing