Registration Header Parameters

Normalized identity and public registration information from FDA records.

Source

FDA Device Registration & Listing

Record Type

Device registration/listing

Registration Number

3009046867

FEI Number

3009046867

Entity Name

Productos Internacionales MABE SA DE CV

City/State/Country

Puebla, MX

Establishment Address

Av. San Pablo Xochimehuacan 7213 Colonia La Loma, Puebla 72230, MX

Establishment Type(s)

Manufacture Medical Device for Another Party (Contract Manufacturer),Manufacture Medical Device

Owner / Operator

PRODUCTOS INTERNACIONALES MABE SA DE CV (Owner Number: 10094938)

Owner / Operator Contact Address

Blvd. Atlixcayotl 3192 Piso 3 (303 - 304), Col. San Martinito, San Andrés Cholula, Puebla, MX-PUE 72825, MX

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
EYQ	Garment, Protective, For Incontinence	Gastroenterology, Urology	Class 1	876.5920	2026-01-07
HHD	Pad, Menstrual, Unscented	Obstetrics/Gynecology	Class 1	884.5435	2026-01-07

Official Correspondent

No official correspondent registered.

US Agent Details

Steven Gonzalez Business: Hyman, Phelps & McNamara PC Email: USAgent-Softys@hpm.com Phone: (202) 7375600

Related Public Records

Same Entity

PRODUCTOS INTERNACIONALES MABE SA DE CV

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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3010048541	ABENA NORTH AMERICA, INC.	Oceanside, CA, US
3016452317	GUANGDONG CHUANTIAN SANITARY PRODUCTS CO.,LTD	Zhongshan Guangdong, CN
3012162353	INTELLIGENT FABRIC TECHNOLOGIES (NORTH AMERICA) INC.	Markham Ontario, CA

Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3009046867. Last updated year: 2026. Please use registration number 3009046867 when referencing this establishment in official correspondence.