RODENSTOCK HEP 410 1.67 - Indonesia BPOM Medical Device Registration
RODENSTOCK HEP 410 1.67 is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11204320940. 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 PT. SOURCE OF KENCANA BLESSINGS.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
RODENSTOCK (THAILAND) CO., LTDCountry of Origin
Thailand
Authorized Representative
PT. SOURCE OF KENCANA BLESSINGSAR Address
JL. KS. TUBUN RAYA NO. 64,
Registration Date
Aug 17, 2023
Expiry Date
Feb 14, 2028
Product Type
Therapeutic Eye Equipment
Prescription show lens.
Non Electromedic Non Sterile
HEP Perfalit 1.74
RODENSTOCK SV 1.60 CM3 HT
RODENSTOCK SF CM3 1.67
RODENSTOCK IPR B.I.G NORM
RODENSTOCK HEP PERFALIT 1.50
HEP CM3 1.54
HEP CM3 1.60
PROG SI 1.5
RODENSTOCK TL 1.50 D60 - 1.75 dpt. Perfalit
HEP 410 1.60
WlDEX MOMENT MRRLD 330
WSAUD A/S
WIDEX MOMENT MRRLD 110
WSAUD A/S
RODENSTOCK SF CM3 1.60
RODENSTOCK (THAILAND) CO., LTD.
RODENSTOCK SV 1.60 CM3 HT
RODENSTOCK (THAILAND) CO., LTD
RODENSTOCK SF CM3 1.67
RODENSTOCK (THAILAND) CO., LTD
WIDEX MOMENT MRR4D 330
WSAUD A/S
WIDEX MOMENT MRR4D 220
WSAUD A/S
WIDEX MOMENT MRR4D 440
WSAUD A/S
RODENSTOCK IPR B.I.G NORM
RODENSTOCK (THAILAND) CO., LTD
WIDEX MOMENT MRR4D 110
WSAUD A/S