MEDAX S.R.L. UNIPERSONALE

FDA Device Registration & Listing · San Possidonio Modena, IT · Registration 3007648417

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
3007648417
FEI Number
3007648417
Entity Name
MEDAX S.R.L. UNIPERSONALE
City/State/Country
San Possidonio Modena, IT
Establishment Address
Via Sandro Pertini 4, San Possidonio Modena 41039, IT
Establishment Type(s)
Manufacture Medical Device
Owner / Operator
Medax S.r.l. Unipersonale (Owner Number: 10029412)
Owner / Operator Contact Address
Via S.Pertini , 4, San Possidonio, IT-MO 41039, IT
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
PMA Number
N/A

All Registered Proprietary Names

MED-GUIDE 1 MEDEXTRA MEDONE ULTRA SINUREP MEDWIRE MEDBONE MEDCUT MEDEM MEDLOCK MEDONE FNA WESTCOTT LUX 2 PERFECTUS FACILE UNIVERSAL PLUS NEO OXUS HANDLEX UNIVERSAL VELOX LUX MEDEASY HEMAX VELOX 2 FNA CHIBA CAESAR HEPAX UNIVERSAL DUO FNA FRANSEEN MED-J MED-S MED-B MED-L MED-I BIO-FEATHER COX AVANGARDE

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
OIJ Biopsy Needle Guide Kit Radiology Class 2 892.1560 2024-07-22
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2020-04-06
MIJ Needle, Tumor Localization General, Plastic Surgery Class 1 878.4800 2017-11-16
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2017-11-27
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2018-11-12
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2020-04-06
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2016-02-03

Official Correspondent

Francesco Elia Sansonne

US Agent Details

Michael C Ryan Email: mcryan913@gmail.com Phone: (724) 7130151

Related Public Records

Same Entity

Medax S.r.l. Unipersonale
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
K172344 Medax Srl Unipersonale Medax Biopsy Systems II (MEDONE, MEDCUT, MEDEM, MEDBONE, MEDLOCK) 2017-11-13

Related Recall Records

Recall ID Recalling Firm Recall Class Product Description
Z-0027-2024 Bard Peripheral Vascular Inc 2
Bard Marquee Disposable Core Biopsy Instrument Kit, REF: MQK2016
Z-0028-2013 Remington Medical Inc. 2
Automatic Cutting Needles, Soft Tissue Biopsy Needle, NAC-1820M, Sterile, Remington Medical, Inc., 5830 Meadowridge Court, Alpharetta, GA 30005. Prostate Biopsy Needles shall be single use only and are to be used by a Urologist in a healthcare setting to obtain needle biopsies of the prostate. The needles are compatible with the Bard Magnum biopsy instrument. The needles have an echogenic tip for accurate placement under ultrasound guidance and centimeter markings along the cannula to facilitate depth placement.
Z-0042-2014 Atossa Genetics, Inc. 2
Brand: The ForeCYTE Breast Health Test, Mammary Aspiration Specimen Cytology Test (MASCT), MASCT System Kits, Clarity System Kits, MASCT Patient Sample Kits & Clarity Patient Sample Kits Instrument, Biopsy. The MASCT System Kit, Patient Sample Kits, or the Nipple Aspirate Fluid Laboratory Kit has the following codes: PRODUCT CODE: AG-MASCT; AG-FC5; DTG-MASCT, DTG-FC5, and NRLBH-5. PART NUMBER: 9002513; 9002513MD; 9002528; 9002528MD; 9002587; 9002614; and 9002717MD. THE MASCT SYSTEM KIT CONSISTS OF: 1. MASCT Breast Pump; 2. Instructions for Use (IFU); 3. Heating Pad; 4. Timer; 5. Saccomono's Fixative; 6. Nu Prep Gel; 7. Welcome and Training Materials Coversheet; 8. MASCT System Order Form; 9. ForeCYTE Training Video DVD; 10. MASCT System Instructions with pictures - pink; THE PATIENT SAMPLE KIT CONSISTS OF: 1. Two (2) flower assemblies (e.g., filter, filter retainer, and filter holder); 2. Instructions for Use (IFU); 3. Two (2) specimen collection devices; 4. Two (2) breast bags for transporting the specimen collection container; 5. Barcode labels; 6. Saccomono's Fixative; 7. Nu Prep Gel; 8. MASCT System package insert; 9. ForeCYTE Test Requisition Form; 10. Patient Information Sheet; 11. Atossa Patient Information; 12. FED EX Clinical PAK; 13. MASCT System Order Form; 14. FED EX Pouch; 15. FED EX Airbill; Product Usage: The MASCT Device is intended for use in the collection of nipple aspirate fluid for cytological testing. The collected fluid can be used in the determination and/or differentiation of normal versus premalignant versus malignant cells.
Z-0044-2018 Bard Peripheral Vascular Inc 2
BARD MAX-CORE Disposable Core Biopsy Instrument, Product Codes - MC1410, 14 g x 10 cm; MC1616, 16 g x 16 cm; MC1816, 18 g x 16 cm; MC1820, 18 g x 20 cm; MC1825, 18 g x 25 cm. The core needle biopsy device is intended for use in obtaining biopsies from soft tissues.

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Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3007648417. Last updated year: 2026. Please use registration number 3007648417 when referencing this establishment in official correspondence.
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