Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3017830316

FEI Number

3017830316

Entity Name

bioBoaVista

City/State/Country

Valinhos Sao Paulo, BR

Establishment Address

contato@bioboavista.com.br, Valinhos Sao Paulo 13273-200, BR

Establishment Type(s)

Manufacture Medical Device

Owner / Operator

ALB LUZ (Owner Number: 10079096)

Owner / Operator Contact Address

Rua Um, 437, Valinhos, BR-SP 13273-200, BR

Initial Importer Flag

Expiration Date (Year)

2026

510(k) Number

N/A

PMA Number

N/A

All Registered Proprietary Names

No proprietary names listed under this establishment.

Registered Product Listings

Product Code	Device Name	Medical Specialty	Device Class	Regulation Number	Created Date
LIO	Device, Specimen Collection	Microbiology	Class 1	866.2900	2020-11-18
QMC	Transport Medium, Notified Per The Vtm Guidance	Microbiology	Class 1	866.2390	2021-03-15
KXG	Applicator, Absorbent Tipped, Sterile	General Hospital	Class 1	880.6025	2021-02-23

Official Correspondent

Ana Luiza Bueno Luz

US Agent Details

PASSARINI CRO AND REGULATORY SOLUTIONS LLC Email: usagent@passarini.com.br Phone: (786) 8496760

Related Public Records

Same Entity

ALB LUZ

View consolidated registration, premarket clearance, and recall records for this applicant.

View Entity Profile →

Related 510(k) Records

510(k) Number	Applicant	Device Name	Decision Date
K003761	Medical Packaging Corp.	NAT - NUCLEIC ACID TRANSPORT	2001-05-31

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3017830316. Last updated year: 2026. Please use registration number 3017830316 when referencing this establishment in official correspondence.