Silgan Dispensing Systems Hemer G M B H

FDA Filings

This page includes the latest FDA filings for Silgan Dispensing Systems Hemer G M B H. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

FDA Registration(s)
Registration Number8010692
FEI Number3007056352
NameSilgan Dispensing Systems Hemer GmbH
Owner & OperatorSilgan Dispensing Systems Germany GmbH
Contact AddressErnst-Stenner-Strasse 17 --
Hemer DE-NOTA 58675 DE
US Agent
Registration Status1
Initial ImporterN
Registration Expiration2020-04-25
Registration AddressERNST-STENNER-STRASSE 17
HEMER Nordrhein-Westfalen, 58675 DE
Establishment TypeManufacture Medical Device

FDA Filings

Device
Company
DeviceDate
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
Iridya Eye Dropper2019-11-28
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
PFP1984-06-07
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
Mark VII Max1984-06-07
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
MK1984-06-07
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
MISTETTE1984-06-07
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
MARK II1984-06-07
Silgan Dispensing Systems Hemer GmbH [Silgan Dispensing Systems Germany GmbH]
HiMark CR1984-06-07

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