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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 16 of 31
DeviceModel / ReferenceRegistriesClassStatus
Midmark DCV5-G2A/H/S2
FDA UDI
Class IIActive
Midmark 153906-016
FDA UDI
Class IUnknown
Midmark P7016V-P
FDA UDI
Class IIActive
Midmark PREVA IntraOral Dental X-ray System DCD5DE‐W1X/H/S1
FDA UDI
Class IIActive
Midmark TRML-L
FDA UDI
Class IActive
Ritter 9A51001-846
FDA UDI
Class IActive
Midmark P22/CV3R
FDA UDI
Class IActive
Midmark 9A386001-851
FDA UDI
Class IActive
Midmark 9A394001-851
FDA UDI
Class IActive
Midmark 9A382001-864
FDA UDI
Class IActive
Ritter 9A337001-867
FDA UDI
Class IActive
Preva, 66" Reach Export W/Two Stud Mount PE7016-P
FDA UDI
Class IIActive
Midmark M9-041 / 9A599001
FDA UDI
Class IIActive
Ritter M11-042
FDA UDI
Class IIActive
Midmark XSVS-0B/L
FDA UDI
Class IIActive
Midmark PREVA 2.0 IntraOral Dental X-ray System DCD7-W1B
FDA UDI
Class IIActive
Midmark PREVA 2.0 IntraOral Dental X-ray System DCD5-W2A
FDA UDI
Class IIActive
Ritter M11 Ultraclave M11-022
FDA UDI
Class IIActive
Ritter 9A329004
FDA UDI
Class IActive
Midmark PREVA IntraOral Dental X-ray System DCD5-W2B/SB
FDA UDI
Class IIActive
Midmark 9A394001-232
FDA UDI
Class IActive
Midmark 9A388001-999
FDA UDI
Class IActive
Midmark 029-7244-04
FDA UDI
Class IActive
Ritter 9A350003
FDA UDI
Class IActive
Midmark 9A390001-851
FDA UDI
Class IActive
Midmark IQecg® Digital ECG 4-000-0062
FDA UDI
Class IIActive
Midmark 9A428001
FDA UDI
Class IActive
Midmark Intraoral Digital Sensor XSVS-06/L
FDA UDI
Class IIActive
Midmark 9A684001-813
FDA UDI
Class IActive
Midmark DCV6-G2X/H/S4
FDA UDI
Class IIActive
Midmark 153905-002
FDA UDI
Class IActive
Midmark 153901-005
FDA UDI
Class IActive
Midmark M3-040
FDA UDI
Class IIActive
Midmark 9A390001-862
FDA UDI
Class IActive
Midmark 9A684001-813
FDA UDI
Class IActive
Midmark DCV7-G2X/H/S1
FDA UDI
Class IIActive
Midmark 630-013
FDA UDI
Class IActive
Midmark G10
FDA UDI
Class IActive
Midmark CV10
FDA UDI
Class IActive
Midmark 9A394001-843
FDA UDI
Class IActive
Midmark P52SC/CV10
FDA UDI
Class IActive
Midmark 9A378001-846
FDA UDI
Class IActive
Midmark 9A684001-813
FDA UDI
Class IActive
Midmark 9A394001-869
FDA UDI
Class IActive
Midmark P22/P3
FDA UDI
Class IActive
Midmark IQvitals Zone, Non-Wireless with Nellcor SPO2
FDA UDI
Class IIActive
Midmark 9A390001-865
FDA UDI
Class IActive
Disposable Spirometer Mouthpieces 2-100-1207
FDA UDI
Class IIActive
Midmark G14
FDA UDI
Class IActive
Midmark PREVA IntraOral Dental X-ray System DCD5-W2M/H/S2
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.

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.