JOHN WEISS Forceps - Indonesia BPOM Medical Device Registration
JOHN WEISS Forceps is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 11203410617. The device is manufactured by JOHN WEISS & SON LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. TRIASTRI MEDITAMA.
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Risk Classification
Product Class
Kelas : 1
Manufacturer
JOHN WEISS & SON LTD.Country of Origin
United Kingdom
Authorized Representative
PT. TRIASTRI MEDITAMAAR Address
GRIYA KEMAYORAN BLOK R-41 JL. INDUSTRI RAYA NO. 9-11
Registration Date
Jul 09, 2021
Expiry Date
Mar 09, 2026
Product Type
Surgical Eye Equipment
Manual ophthalmic surgical instrument.
Non Electromedic Non Sterile
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