TEMED

FDA Device Registration & Listing · Sidlesham West Sussex, GB · Registration 3014247825

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
3014247825
FEI Number
3014247825
Entity Name
TEMED
City/State/Country
Sidlesham West Sussex, GB
Establishment Address
Unit 3 Keynor Farm, Keynor Lane, Sidlesham West Sussex PO20 7LL, GB
Establishment Type(s)
Export Device to the United States But Perform No Other Operation on Device,Develop Specifications But Do Not Manufacture At This Facility
Owner / Operator
TEMED (Owner Number: 10057063)
Owner / Operator Contact Address
Unit 3, Keynor Farm, Keynor Lane, Sidlesham, GB-WSX PO20 7LL, GB
Initial Importer Flag
N
Expiration Date (Year)
2026
510(k) Number
N/A
PMA Number
N/A

All Registered Proprietary Names

TEMED Gas Diffuser TEMED Sucker Line TEMED Mini Sucker

Registered Product Listings

Product Code Device Name Medical Specialty Device Class Regulation Number Created Date
HIF Insufflator, Laparoscopic Obstetrics/Gynecology Class 2 884.1730 2018-02-16
DTS Sucker, Cardiotomy Return, Cardiopulmonary Bypass Cardiovascular Class 2 870.4420 2022-11-28

Official Correspondent

Katie Evans

US Agent Details

Mike Schroeder Business: Med Alliance Group INC Email: mschroeder@medalliancegroup.com Phone: (630) 4437070

Related Public Records

Same Entity

TEMED
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
K981334 Richard Wolf Medical Instruments Corp. LAPARO CO2-PNEU (AND WITH VIDEO MONITORING) 1998-09-10

Similar Registrations

Registration Number Establishment Name Location
1057358 RG Medical USA Mount Juliet, TN, US
1225798 ATC TECHNOLOGIES INC. Wilmington, MA, US
9610612 AESCULAP AG TUTTLINGEN, DONAU Baden-Wurttemberg, DE
1320894 CONMED CORPORATION Utica, NY, US
3001556604 Novanta Medical GmbH BERLIN, DE
Source Citation & Summary: This public preview is extracted from openFDA device registration and listing logs under registration number 3014247825. Last updated year: 2026. Please use registration number 3014247825 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.