Pure Global

ENRAF NONIUS Manumed Tilt - Indonesia BPOM Medical Device Registration

ENRAF NONIUS Manumed Tilt is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21402912431. The device is manufactured by ENRAF NONIUS B.V. from Netherlands, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. MURTI INDAH SENTOSA.

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 : B
ENRAF NONIUS Manumed Tilt
Analysis ID: AKL 21402912431

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

ENRAF NONIUS B.V.

Country of Origin

Netherlands

Authorized Representative

PT. MURTI INDAH SENTOSA

AR Address

WISMA MURTI JL. SULTAN ISKANDAR MUDA KAV. 29 ARTERI PONDOK INDAH

Registration Date

Jul 26, 2023

Expiry Date

Dec 31, 2025

Product Type

Prosthetic Physical Health Equipment

Powered table.

Non Radiation Electromedics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing