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Midmark Corporation

United States·US-MF-000002581

Last updated September 17, 2026

About

Midmark is a global manufacturer and supplier of healthcare products, equipment and diagnostic software for medical, veterinary, and dental markets.

From the manufacturer's own website. Source

Information

Country
United States
Address
60, Vista Drive, Versailles, United States
Phone
—
PRRC Contact
Adam Clutter
EUDAMED SRN
US-MF-000002581
FDA FEI Number
1523530
DUNS Number
—

Catalogue (1527)

Page 31 of 31
DeviceModel / ReferenceRegistriesClassStatus
Midmark 9A82001-844
EUDAMEDFDA UDI
Class IActive
Midmark 9A500001-845
EUDAMEDFDA UDI
Class IActive
Midmark 9A496001-867
EUDAMEDFDA UDI
Class IActive
Midmark 9A81001-866
EUDAMEDFDA UDI
Class IActive
Midmark 9A512001-848
EUDAMEDFDA UDI
Class IActive
Ritter 9A70000
EUDAMEDFDA UDI
Class IActive
Midmark 9A684001-863
EUDAMEDFDA UDI
Class IActive
Midmark 9A496001-999
EUDAMEDFDA UDI
Class IActive
Midmark 9A81001-868
EUDAMEDFDA UDI
Class IActive
Midmark 630-012
EUDAMEDFDA UDI
Class IActive
Midmark 630-022
EUDAMEDFDA UDI
Class IActive
Midmark 9A500001-852
EUDAMEDFDA UDI
Class IActive
Midmark 9A684001-847
EUDAMEDFDA UDI
Class IActive
Midmark 9A81001-865
EUDAMEDFDA UDI
Class IActive
Midmark 9A82001-868
EUDAMEDFDA UDI
Class IActive
Midmark 9A684001-814
EUDAMEDFDA UDI
Class IActive
Midmark 9A157003
EUDAMEDFDA UDI
Class IActive
Midmark 9A600002
EUDAMEDFDA UDI
Class IActive
Midmark 9A81001-852
EUDAMEDFDA UDI
Class IActive
Midmark 9A627001
EUDAMEDFDA UDI
Class IActive
Ritter 9A632001
EUDAMEDFDA UDI
Class IActive
Midmark 9A684001-856
EUDAMEDFDA UDI
Class IActive
Midmark 9A500001-847
EUDAMEDFDA UDI
Class IActive
Midmark 9A82001-862
EUDAMEDFDA UDI
Class IActive
Midmark 9A81001-855
EUDAMEDFDA UDI
Class IActive
Midmark 9A82001-848
EUDAMEDFDA UDI
Class IActive
Midmark 9A512001-862
EUDAMEDFDA UDI
Class IActive

Related Companies

Authorised Representatives

Importers

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Notified Bodies

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Authorities

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FDA Recalls (1)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Mar 5, 2003Z-0704-03—terminated

The pressure relief valve may fail to open properly.