Pure Global

ALTECH Neoprene Breathing Bag - Indonesia BPOM Medical Device Registration

ALTECH Neoprene Breathing Bag is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403027378. The device is manufactured by MEDITERA TIBBI MALZEME SAN. VE T.S. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. SURGIKA ALKESINDO.

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
ALTECH Neoprene Breathing Bag
Analysis ID: AKL 20403027378

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. SURGIKA ALKESINDO

AR Address

Jl. Letjen Suprapto No.60, Gedung Indra Sentral unit G-H, Cempaka Putih

Registration Date

Sep 01, 2022

Expiry Date

Dec 30, 2027

Product Type

Therapeutic Anesthesia Equipment

Reservoir bag.

Non Electromedic Non Sterile

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Other Products from MEDITERA TIBBI MALZEME SAN. VE T.S. A.S.
Products from the same manufacturer (2 products)