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ANVISA registration 81521800001Valid until Jul 29, 2029

optical fiber

ANVISA Registration Number: 81521800001BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-MEG.N.S. NEOLASER LTD.Risk Class III
Verified
Device names
Technical name
optical fiber
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PT: fibra optica
Commercial name
Kit Cânula PLDD
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Risk class
Class III
Registration details
Registration Number
81521800001
Process Number
25351228531202220
CNPJ
27622775000155
Company information
Registration Holder
BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME
Manufacturer
G.N.S. NEOLASER LTD.
Manufacturing Country
Israel
PT: ISRAEL
Dates and status
Publication Date
Apr 18, 2022
Validity
29/07/2029
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for optical fiber in Brazil's medical device market through Pure Global AI's free database. This Risk Class III medical device is registered under ANVISA number 81521800001 and manufactured by G.N.S. NEOLASER LTD.. The registration is held by BPF MEDICAL DISTRIBUIDORA E IMPORTADORA DE PRODUTOS MEDICOS LTDA-ME with validity until Jul 29, 2029.

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.