RUSCH PE Guedel Airways - Indonesia BPOM Medical Device Registration
RUSCH PE Guedel Airways is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20403420682. The device is manufactured by FOREMOUNT ENTERPRISE CO., LTD. from Taiwan (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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
FOREMOUNT ENTERPRISE CO., LTD.Country of Origin
Taiwan (China)
Authorized Representative
TELEFLEX MEDICAL INDONESIAAR Address
Wisma 46 - Kota BNI Lantai 47, Units 01-04, Jl. Jend. Sudirman Kav. 1
Registration Date
Oct 11, 2024
Expiry Date
Nov 14, 2028
Product Type
Therapeutic Anesthesia Equipment
Oropharyngeal airway.
Non Electromedic Sterile
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INDOMEDIPRO Scented Face Mask
INDOMEDIPRO Catheter Mounts
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ACCUMED CORP.
RUSCH Crystal Clear Tracheostomy Cannula
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RUSCH PVC Guedel Airway
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RUSCH Intubation Stylet
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RUSCHELIT Safety Clear Plus Tracheal Tube
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RUSCH RUSCHELIT Super Safety Clear Plus Tracheal Tube Cuffed
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RUSCHELIT Safety Clear Plus Tracheal Tube, without cuff
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ARROW EZ-IO Power Driver
SPARโWATERTOWN, 2012
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RUSCH Tracheofix Tracheostomy Tube Set
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