HEP Perfalit 1.74 - Indonesia BPOM Medical Device Registration
HEP Perfalit 1.74 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204420371. 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
Aug 04, 2024
Expiry Date
Apr 25, 2028
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
RODENSTOCK SV 1.60 CM3 HT
RODENSTOCK SF CM3 1.67
RODENSTOCK IPR B.I.G NORM
RODENSTOCK HEP PERFALIT 1.50
RODENSTOCK HEP 410 1.67
HEP CM3 1.54
RODENSTOCK TL 1.50 D60 - 1.75 dpt. Perfalit
HEP CM3 1.60
PROG SI 1.5
HEP PERFALIT 1.67
WIDEX MOMENT MRRLD 440
WSAUD A/S
IMPACT SP R D 440
WSAUD A/S
WlDEX MOMENT MRRLD 220
WSAUD A/S
IMPACT SP R D 220
WSAUD A/S
PROG SI 1.5
RODENSTOCK (THAILAND) CO., LTD
HEP 410 1.60
RODENSTOCK (THAILAND) CO., LTD
HEP PERFALIT 1.67
RODENSTOCK (THAILAND) CO., LTD
WIDEX MAGNIFY M-XP
WIDEX A/S
WIDEX MAGNIFY MBB3D
WIDEX A/S
WIDEX MOMENT MBB2
WIDEX A/S