A Vitan Inserter folder - Indonesia BPOM Medical Device Registration
A Vitan Inserter folder is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 21203123122. The device is manufactured by DUCKWORTH & KENT, LTD. from United Kingdom, and is classified as Risk Class Kelas Resiko : A. The authorized representative in Indonesia is PT. BRIDGE TWO.
This page provides comprehensive regulatory information including complete registration details, manufacturer information, authorized representative details, product classification, and related products. Pure Global AI offers free access to 67,600+ Indonesia medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.
UNFOLDER Vitan Inserter
Risk Classification
Product Class
Kelas : 1
Manufacturer
DUCKWORTH & KENT, LTD.Country of Origin
United Kingdom
Authorized Representative
PT. BRIDGE TWOAR Address
Jl. Petojo Melintang No. 17
Registration Date
Dec 12, 2024
Expiry Date
Aug 19, 2027
Product Type
Surgical Eye Equipment
Intraocular lens guide
Non Electromedic Non Sterile
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TECHNOCLONE Fibrinogen Reagent Kit
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APPLIED MEDICAL RESOURCES CORPORATION
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HTL-STREFA S.A.

