BARD PTFE Felt - Indonesia BPOM Medical Device Registration
BARD PTFE Felt is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20503712969. The device is manufactured by BARD SHANNON LIMITED from United States, and is classified as Risk Class Kelas Resiko : C. The authorized representative in Indonesia is PT. GEM OF MOTHER ARTANO.
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.
Risk Classification
Product Class
Kelas : 2
Manufacturer
BARD SHANNON LIMITEDCountry of Origin
United States
Authorized Representative
PT. GEM OF MOTHER ARTANOAR Address
Jl. Hos. Cokroaminoto, Komp. Perkantoran CBD Ciledug Blok A3 No. 17, Ciledug 15157
Registration Date
May 16, 2023
Expiry Date
Feb 10, 2028
Product Type
Prosthetic Cardiology Equipment
Intracardiac patch or pledget made of polypropylene, polyethylene terephthalate, or polytetrafluoroethylene.
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FEHLING INSTRUMENTS Aspirators
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FEHLING INSTRUMENTS Retractors III
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FEHLING INSTRUMENTS Holding and Guiding Instruments
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FEHLING INSTRUMENTS Aortic Punches
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FEHLING INSTRUMENTS Gauges and Sizing Instruments
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FEHLING INSTRUMENTS Forceps I
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FEHLING INSTRUMENTS Dissectors
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FEHLING INSTRUMENTS Clamps II
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FEHLING INSTRUMENTS Forceps III
FEHLING INSTRUMENTS GMBH & CO. KG.

