FAMILIA DEL PACIFICO SAS

FDA Device Registration & Listing · Guachene Cauca, CO · Registration 3005202853

Public Record Device Listing Expiry Year: 2026 This page presents structured fields from public FDA datasets.

Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source
FDA Device Registration & Listing
Record Type
Device registration/listing
Registration Number
3005202853
FEI Number
3005202853
Entity Name
FAMILIA DEL PACIFICO SAS
City/State/Country
Guachene Cauca, CO
Establishment Address
ZONA FRANCA PERMANENTE DEL CAUCA, PARQUE INDUSTRIAL Y COMERCIAL DEL CAUCA VIA GUACHENE, Guachene Cauca -, CO
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
FAMILIA DEL PACIFICO S.A.S (Owner Number: 10027740)
Owner / Operator Contact Address
Metro Office Park Calle 1 Edificio 7, Ofic 303, Guaynabo, PR 00968, US
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

Nice Day Nosotras TENA SLIP ULTRA PROTECT Tena Nosotras Nice Day Nosotras Nice Day Tena

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
EYQ Garment, Protective, For Incontinence Gastroenterology, Urology Class 1 876.5920 2008-11-28
NRC Pad, Menstrual, Scented, Scented-Deodorized Made Of Common Cellulosic & Synthetic Material W/Established Safety Profile Obstetrics/Gynecology Class 1 884.5425 2008-11-28
HHD Pad, Menstrual, Unscented Obstetrics/Gynecology Class 1 884.5435 2008-11-28

Official Correspondent

Adriana Navarro

US Agent Details

Monica Cabrera Business: Tradeworks Email: mcabrera@tradeworkspr.com Phone: (787) 9571230

Related Public Records

Same Entity

FAMILIA DEL PACIFICO S.A.S
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
K823241 Kimberly-Clark Corp. NEW FREEDOM THIN UNSCENTED MAXI PADS 1982-12-28

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3005202853. Last updated year: 2026. Please use registration number 3005202853 when referencing this establishment in official correspondence.
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