Andersen Caledonia L T D

FDA Filings

This page includes the latest FDA filings for Andersen Caledonia L T D. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number3004530184
FEI Number3004530184
NameANDERSEN CALEDONIA LTD
Owner & OperatorAndersen Caledonia Ltd
Contact AddressCaledonian House, Phoenix Crescent Strathclyde Business Park
Bellshill GB-SCT Scotland ML4 3NJ GB
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressCaledonian House, Phoenix Crescent Strathclyde Business Park
Bellshill Scotland, ML4 3NJ GB
Establishment TypeSterilize Medical Device for Another Party (Contract Sterilizer)

FDA Filings

Device
Company
DeviceDate
ANDERSEN CALEDONIA LTD
TRP001 - Dispoable Treatment Pipe2019-08-28
ANDERSEN CALEDONIA LTD
DSP003 - Large Disposable Speculum2019-08-28
ANDERSEN CALEDONIA LTD
DSP002 - Medium Disposable Speculum2019-08-28
ANDERSEN CALEDONIA LTD
DSP001 - Small Disposable Speculum2019-08-28
ANDERSEN CALEDONIA LTD
OpClear? System2019-08-04
ANDERSEN CALEDONIA LTD
OpClear? System2019-08-04
ANDERSEN CALEDONIA LTD
LBF 0062017-12-06
ANDERSEN CALEDONIA LTD
Lotus Series 4 Ultrasonic Surgical System & Accessories2017-01-27

Related Finance Registrations
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.