R-VENT MEDIKAL URETIM A.S.

FDA Device Registration & Listing · TORBALI Izmir, TR · Registration 3013659051

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
3013659051
FEI Number
3013659051
Entity Name
R-VENT MEDIKAL URETIM A.S.
City/State/Country
TORBALI Izmir, TR
Establishment Address
YAZIBASI MAHALLESI BALKAN CADDESI IZTIPSAN APT.NO:33/1, TORBALI Izmir 35875, TR
Establishment Type(s)
Manufacture Medical Device,Sterilize Medical Device for Another Party (Contract Sterilizer),Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
R-Vent Medikal Uretim A.S. (Owner Number: 10062535)
Owner / Operator Contact Address
YAZIBASI MAHALLESI BALKAN CADDESI IZTIPSAN APT.NO:33/1, TORBALI, TR-35 35875, TR
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

R Vent

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
BZO Set, Tubing And Support, Ventilator (W Harness) Anesthesiology Class 1 868.5975 2020-04-01

Official Correspondent

AHMET SAHIN

US Agent Details

Joseph Consoli Business: Sunset Healthcare Solutions Inc. Email: jconsoli@sunsethcs.com Phone: (773) 5190969

Related Public Records

Same Entity

R-Vent Medikal Uretim A.S.
View consolidated registration, premarket clearance, and recall records for this applicant.
View Entity Profile →

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0031-2026 Percussionaire Corporation 1
Phasitron 5, IPV In-Line Valve, (Intrapulmonary Percussive Ventilation) REF: P5-TEE-20 (pack of 20)/ P5-TEE (individual) with In-Line Valve Sentec Instructions for Use

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3013659051. Last updated year: 2026. Please use registration number 3013659051 when referencing this establishment in official correspondence.
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