Pure Global

MDF 808 Professional Aneroid Sphygmomanometer - Indonesia BPOM Medical Device Registration

MDF 808 Professional Aneroid Sphygmomanometer is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20501806218. The device is manufactured by MDF INSTRUMENTS MEDIFRIEND, INC. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. FA ANTARES MEDIKA.

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
MDF 808 Professional Aneroid Sphygmomanometer
Analysis ID: AKL 20501806218

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

PT. FA ANTARES MEDIKA

AR Address

Ruko Golden Boulevard Blok i No 7 BSD City

Registration Date

Feb 24, 2022

Expiry Date

Dec 28, 2026

Product Type

Diagnostic Cardiology Equipment

Noninvasive blood pressure measurement system.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from MDF INSTRUMENTS MEDIFRIEND, INC.
Products from the same manufacturer (1 products)