HEP 410 1.60 - Indonesia BPOM Medical Device Registration
HEP 410 1.60 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204320855. The device is manufactured by RODENSTOCK (THAILAND) CO., LTD from Thailand, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is SOURCE OF KENCANA BLESSINGS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
RODENSTOCK (THAILAND) CO., LTDCountry of Origin
Thailand
Authorized Representative
SOURCE OF KENCANA BLESSINGSAR Address
JL. KS. TUBUN RAYA NO. 64,
Registration Date
Jul 25, 2023
Expiry Date
Apr 25, 2028
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
HEP Perfalit 1.74
RODENSTOCK SF CM3 1.67
RODENSTOCK SV 1.60 CM3 HT
RODENSTOCK IPR B.I.G NORM
RODENSTOCK HEP PERFALIT 1.50
RODENSTOCK HEP 410 1.67
RODENSTOCK TL 1.50 D60 - 1.75 dpt. Perfalit
HEP CM3 1.60
PROG SI 1.5
HEP CM3 1.54
WIDEX MOMENT MRRLD 440
WSAUD A/S
IMPACT SP R D 440
WSAUD A/S
WlDEX MOMENT MRRLD 220
WSAUD A/S
HEP Perfalit 1.74
RODENSTOCK (THAILAND) CO., LTD
IMPACT SP R D 220
WSAUD A/S
PROG SI 1.5
RODENSTOCK (THAILAND) CO., LTD
HEP PERFALIT 1.67
RODENSTOCK (THAILAND) CO., LTD
WIDEX MAGNIFY MBB3D
WIDEX A/S
WIDEX MAGNIFY M-XP
WIDEX A/S
WIDEX MOMENT MBB2
WIDEX A/S