INFUS MEDICAL (THAILAND) CO., LTD.

FDA Device Registration & Listing · Amphoe Muang Samutprakarn Samut Prakan, TH · Registration 9680340

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
9680340
FEI Number
1000434163
Entity Name
INFUS MEDICAL (THAILAND) CO., LTD.
City/State/Country
Amphoe Muang Samutprakarn Samut Prakan, TH
Establishment Address
706 MOO 4, Bangpoo Industrial Estate, I-EA-T Free Zone, Tambon Preaksa, Amphoe Muang Samutprakarn Samut Prakan 10280, TH
Establishment Type(s)
Manufacture Medical Device for Another Party (Contract Manufacturer)
Owner / Operator
Infus Medical (Thailand) Co., Ltd. (Owner Number: 9008323)
Owner / Operator Contact Address
706 Moo 4, Bangpoo Industrial Estate,, I-EA-T Free Zone, T. Preaksa, A. Muang, Samutprakarn, TH-NOTA 10280, TH
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

SenoRx Inc. SenoRx Inc. EnCor MRI Introducer Set TITANIUM HEMOSTATIC CLIP Insufflation Tubing Set, HE+SE+HU SenoRx Inc. CloudCath Peritoneal Dialysis Drain Set Monitoring System

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2023-08-25
HIG Insufflator, Hysteroscopic Obstetrics/Gynecology Class 2 884.1700 2014-01-30
HIF Insufflator, Laparoscopic Obstetrics/Gynecology Class 2 884.1730 2025-06-04
FZP Clip, Implantable General, Plastic Surgery Class 2 878.4300 2007-11-13
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2011-08-12
HIF Insufflator, Laparoscopic Obstetrics/Gynecology Class 2 884.1730 2020-08-13
OSV Insufflator, Endoscopic Vessel Harvesting Obstetrics/Gynecology Class 2 884.1730 2020-08-13
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2011-08-12
GEI Electrosurgical, Cutting & Coagulation & Accessories General, Plastic Surgery Class 2 878.4400 2012-02-24
FZP Clip, Implantable General, Plastic Surgery Class 2 878.4300 2012-01-18
HIF Insufflator, Laparoscopic Obstetrics/Gynecology Class 2 884.1730 2025-09-30
KNW Instrument, Biopsy Gastroenterology, Urology Class 2 876.1075 2012-01-04
HIF Insufflator, Laparoscopic Obstetrics/Gynecology Class 2 884.1730 2013-06-07
HRX Arthroscope Orthopedic Class 2 888.1100 2013-06-07
HRX Arthroscope Orthopedic Class 2 888.1100 2015-01-15
NEU Marker, Radiographic, Implantable General, Plastic Surgery Class 2 878.4300 2011-08-12
FKX System, Peritoneal, Automatic Delivery Gastroenterology, Urology Class 2 876.5630 2022-08-29
HIG Insufflator, Hysteroscopic Obstetrics/Gynecology Class 2 884.1700 2015-01-15

Official Correspondent

Patcharin Vinitwatanakhun

US Agent Details

Jerry Doane Business: Pragmatic Compliance dba FDAbasics Email: usagent@fdabasics.com Phone: (716) 7750533

Related Public Records

Same Entity

Infus Medical (Thailand) Co., Ltd.
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
K905706 Circon Acmi GYN-1500 HYSTEROSCOPIC INUFFLATOR 1991-02-28
K981334 Richard Wolf Medical Instruments Corp. LAPARO CO2-PNEU (AND WITH VIDEO MONITORING) 1998-09-10
K970809 Somnus Medical Technologies, Inc. BENDABLE TISSUE COAGULATING ELECTRODE WITH BENDING TOOL 1997-06-18
K222793 C.R. Bard, Inc. WavelinQ™ Generator 2022-10-17

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.
Z-0031-06 Rita Medical Systems 2
Rita Brand Habib 4X Electrosurgical Coagulator, Catalog Number: 4401US; Product is distributed by RITA Medical Systems, Inc., One Horizon Way. Manchester, GA 32826

Similar Registrations

Registration Number Establishment Name Location
3042940295 NEONAVIA AB Vallentuna Stockholm, SE
3038611181 XAGA SURGICAL AB Eslov Skane, SE
1018233 C.R. BARD, INC. COVINGTON, GA, US
2648623 STERIS ISOMEDIX PUERTO RICO, INC. Alts De Cerro Gordo 3&4, PR, US
3010515547 PROMISEMED HANGZHOU MEDITECH CO.,LTD. Hangzhou Zhejiang, CN
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 9680340. Last updated year: 2026. Please use registration number 9680340 when referencing this establishment in official correspondence.
Legal Disclaimer: AvaSpecs is not affiliated with the FDA or any government agency and does not provide medical, legal, regulatory, safety, approval, clearance, effectiveness, endorsement, or compliance advice. This index page is built using public record archives and does not represent an official regulatory determination.
Account Required Full available specs will require a free AvaSpecs account.