Pure Global

ELECTRO-MAG Incubator M 6040 BP - Indonesia BPOM Medical Device Registration

ELECTRO-MAG Incubator M 6040 BP is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10302700296. The device is manufactured by ELEKTRO-MAG LABORATUVAR ALETLERI SAN. VE TIC. AS. from Turkey, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. ALKESTRON SELF-SOURCE.

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 : A
ELECTRO-MAG Incubator M 6040 BP

ELEKTRO-MAG Incubator M 6040 BP

Analysis ID: AKL 10302700296

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

Turkey

Authorized Representative

PT. ALKESTRON SELF-SOURCE

AR Address

Komp Ruko Griya Inti Sentosa Jln. Griya Agung Blok O No. 95-96

Registration Date

Nov 18, 2022

Expiry Date

Nov 08, 2027

Product Type

Microbiology Equipment

Microbiological incubator.

Invitro Diagnostics

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from ELEKTRO-MAG LABORATUVAR ALETLERI SAN. VE TIC. AS.
Products from the same manufacturer (1 products)