Amcor L T D

FDA Filings

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

Amcor L T D holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number9617111
FEI Number3006442872
NameKailey Check
Owner & OperatorAMCOR, LTD.
Contact Address1919 Butterfiled Road --
Mundelein IL 60060 US
Official Correspondent
  • Kailey Check
  • x-847-9184287-x
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration Address1919 S. Butterfield Rd
Mundelein, IL 60060 US
Establishment TypeManufacture Medical Device



FDA Filings

Device
Company
DeviceDate
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
Kailey Check [AMCOR, LTD.]
TYVEK Pouch/Roll with STERRAD Chemical Indicator2013-02-07
AMCOR, LTD.
SLANT/FIN HEPA CLEAR1995-10-30

Similar & Related FDA Registered Companies

Related Finance Registrations
NCAGE CodeZAZ10AMCOR LTD
NCAGE Code9WBNAAMCOR LTD
CAGE CodeZAZ10AMCOR LTD
CAGE Code9WBNAAMCOR LTD
SEC0000869428AMCOR LTD of AUSTRALIA
SEC0000802720AMCOR LTD /ADR/
SEC0000799381AMCOR LTD /FI

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