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SMART CARE Guedel Airway - Indonesia BPOM Medical Device Registration

SMART CARE Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403321341. The device is manufactured by WELL LEAD MEDICAL CO.,LTD from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SMART CARE 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 : A
SMART CARE Guedel Airway
Analysis ID: AKL 10403321341

Risk Classification

Kelas Resiko : A

Product Class

Kelas : 1

Country of Origin

China

Authorized Representative

PT. SMART CARE INDONESIA

AR Address

RUKO MELATI MAS SQUARE,BLOK A3 NO.8 SERPONG-TANGERANG

Registration Date

Jun 09, 2023

Expiry Date

Jun 07, 2026

Product Type

Therapeutic Anesthesia Equipment

Oropharyngeal airway

Non Electromedic Sterile

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