GULF Surgical Headlight - Indonesia BPOM Medical Device Registration
GULF Surgical Headlight is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21603310645. The device is manufactured by GULF FIBEROPTICS INC from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. GLOBAL SYSTECH MEDIKA.
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Risk Classification
Product Class
Kelas : 2
Manufacturer
GULF FIBEROPTICS INCCountry of Origin
United States
Authorized Representative
PT. GLOBAL SYSTECH MEDIKAAR Address
Jl. TB Simatupang No.17 RT.011/002 Kel. Susukan, Kec. Ciracas Jakarta Timur
Registration Date
Nov 17, 2021
Expiry Date
Feb 22, 2026
Product Type
Surgical Equipment
Surgical lamp.
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