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SEATTLE PAP PLUS System - Indonesia BPOM Medical Device Registration

SEATTLE PAP PLUS System is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403915395. The device is manufactured by ALTERA TIBBI MALZEME SAN. VE TIC. A.S. from Turkey, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. DRAEGER 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.

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BPOM Registered
Risk Class Kelas Resiko : C
SEATTLE PAP PLUS System
Analysis ID: AKL 20403915395

Risk Classification

Kelas Resiko : C

Product Class

Kelas : 2

Country of Origin

Turkey

Authorized Representative

PT. DRAEGER MEDICAL INDONESIA

AR Address

ALAMANDA TOWER Lt. 32 Unit A, B, D, E, F. Jl. TB. Simatupang Kav. 23-24

Registration Date

Jul 27, 2023

Expiry Date

Jul 14, 2027

Product Type

Therapeutic Anesthesia Equipment

Noncontinuous ventilator (IPPB).

Non Electromedic Non Sterile

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