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RUSCH PVC Guedel Airway - Indonesia BPOM Medical Device Registration

RUSCH PVC Guedel Airway is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420482. The device is manufactured by FOREMOUNT ENTERPRISE CO. LTD. from China, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is TELEFLEX 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 : B
RUSCH PVC Guedel Airway
Analysis ID: AKL 20403420482

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Country of Origin

China

Authorized Representative

TELEFLEX MEDICAL INDONESIA

AR Address

Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1

Registration Date

Jul 02, 2024

Expiry Date

Nov 14, 2028

Product Type

Therapeutic Anesthesia Equipment

Oropharyngeal airway.

Non Electromedic Non Sterile

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