PRO-TECH Pro-Flow and Pro-Flow Plus Nasal Cannulas - Indonesia BPOM Medical Device Registration
PRO-TECH Pro-Flow and Pro-Flow Plus Nasal Cannulas is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 10403021138. The device is manufactured by PRO-TECH SERVICES, INC. from United States, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. PHILIPS INDONESIA COMMERCIAL.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
PRO-TECH SERVICES, INC.Country of Origin
United States
Authorized Representative
PT. PHILIPS INDONESIA COMMERCIALAR Address
Gedung Cibis Nine Lantai 10, Jl. T.B. Simatupang No. 2 RT 001 RW 005
Registration Date
Feb 07, 2025
Expiry Date
Oct 30, 2029
Product Type
Therapeutic Anesthesia Equipment
Nasal oxygen cannula.
Non Electromedic Non Sterile
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