Q-MED LEAD GLASS - Indonesia BPOM Medical Device Registration
Q-MED LEAD GLASS is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11503121699. The device is manufactured by SHANDONG DOUBLE EAGLE MEDICAL DEVICE CO., LTD. from China, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. SRI INTAN PERKASA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
SHANDONG DOUBLE EAGLE MEDICAL DEVICE CO., LTD.Country of Origin
China
Authorized Representative
PT. SRI INTAN PERKASAAR Address
RUKO HARAPAN INDAH BLOK EN/7 KOMPLEK HARAPAN INDAH BEKASI BARAT, KOTA BEKASI, JAWA BARAT
Registration Date
Mar 30, 2021
Expiry Date
Mar 26, 2024
Product Type
Other Radiology Equipment
Personnel protective shield.
Non Electromedic Non Sterile
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DOUBLE EAGLE PROTECTIVE GLOVES
DOUBLE EAGLE PROTECTIVE GLASSES PC
DOUBLE EAGLE Lead Apron PA
DOUBLE EAGLE Protective Scrotum
DOUBLE EAGLE Lead Apron PDW
DOUBLE EAGLE PROTECTIVE GLASSES PA
DOUBLE EAGLE PROTECTIVE SCREEN
Q-MED X-Ray Film Cassette
Q-MED X-RAY GRIDS
RMS MDX 300R
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RMS MDX 100M
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RMS HFX 3.5P
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E-JOIN MEDICAL IMAGE PRINTER
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E-JOIN MEDICAL IMAGE PRINTER
E-JOIN (SHENZHEN) TECHNOLOGY LIMITED
Q-MED Protective Gonad
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E-JOIN THERMAL Film
E-JOIN (SHENZHEN) TECHNOLOGY LIMITED
E-JOIN Thermal Film
E-JOIN (SHENZHEN) TECHNOLOGY LIMITED
E-JOIN Thermal Film
E-JOIN (SHENZHEN) TECHNOLOGY LIMITED
Q-MED Protective Cap PD
SHANGDONG DOUBLE EAGLE MEDICAL DEVICE CO., LTD.