Pure Global

DELFIA Neonatal 17 Alfa OH Progesterone Kit - Indonesia BPOM Medical Device Registration

DELFIA Neonatal 17 Alfa OH Progesterone Kit is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20101221194. The device is manufactured by WALLAC OY from Finland, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. UBC MEDICAL INDONESIA.

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
DELFIA Neonatal 17 Alfa OH Progesterone Kit
Analysis ID: AKL 20101221194

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

WALLAC OY

Country of Origin

Finland

Authorized Representative

PT. UBC MEDICAL INDONESIA

AR Address

Jalan Rawa Gelam V, Blok L Kav. 11-13, Kawasan Industri Pulogadung Jakarta Timur13930

Registration Date

Feb 04, 2025

Expiry Date

Oct 22, 2028

Product Type

Clinical Chemistry Test System

17-Hydroxyprogesterone test system (kit & cair)

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Similar Products (1)
Other products with the same name