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.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
FOREMOUNT ENTERPRISE CO. LTD.Country of Origin
China
Authorized Representative
TELEFLEX MEDICAL INDONESIAAR 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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