WIESNER HEALTHCARE SAS

FDA Device Registration & Listing · Medellin Antioquia, CO · Registration 3013548509

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
3013548509
FEI Number
3013548509
Entity Name
WIESNER HEALTHCARE SAS
City/State/Country
Medellin Antioquia, CO
Establishment Address
CRA 9A SUR # 20 - 340, CV64, Medellin Antioquia 050021, CO
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
WIESNER HEALTHCARE SAS (Owner Number: 10054405)
Owner / Operator Contact Address
CRA 9A SUR # 20 - 340, CV64, Medellin, CO-ANT 050021, CO
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

WIESNER Incontinence Clamp VIRTH Lung Expansion and Mucus Relief Device

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
FHA Clamp, Penile Gastroenterology, Urology Class 1 876.5160 2017-03-15
BYP Mouthpiece, Breathing Anesthesiology Class 1 868.5620 2022-10-24

Official Correspondent

No official correspondent registered.

US Agent Details

David Lennarz Business: Registrar Corp Email: david.lennarz@registrarcorp.com Phone: (757) 2240177

Related Public Records

Same Entity

WIESNER HEALTHCARE SAS
View consolidated registration, premarket clearance, and recall records for this applicant.
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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013548509. Last updated year: 2026. Please use registration number 3013548509 when referencing this establishment in official correspondence.
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