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Medrx, Inc.

Active in EUDAMED

United Statesfrom SRN EUDAMED FDA SRN US-MF-000025226 FEI 1000307595

Medrx, Inc. is a medical device manufacturer based in the United States, with 13 devices listed in FDA GUDID, EUDAMED and FDA 510(k) (FDA Class II and I) as of 14 Nov 2026.

Devices
13
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • FDA GUDID 12
  • EUDAMED 8
  • FDA 510(k) 1

A device listed in two registries counts in both.

Device classes
  • FDA Class II 12
  • FDA Class I 1
Identifiers
  • EUDAMED SRN US-MF-000025226
  • FDA FEI 1000307595
  • DUNS 849311261

At a glance

Counted by deviCERTS from registry records

EU certificates

1 of 1 in force.

See certificates

Market reach

European Union
EUDAMED actor, 1 certificate
United States
FDA FEI

Catalogue13

Newest first, rows 1-13 of 13

Search and filter all 13 devices
Skip device list
  • MedRx Avant HIT+

    Listed Registry: GUDID Class:II
  • MedRx Video Otoscope

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:I
  • MedRx Avant REMsp

    Listed Registry: GUDID Class:II
  • MedRx Avant A2D+

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • MedRx Avant REM Speech+

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • MedRx Kiosk

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • MedRx AWRC

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • MedRx Avant ARC

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • MedRx Tinnometer

    Withdrawn Registry: GUDID Class:II
  • MedRx Avant AIR+

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • MedRx WREM

    Active Regimes: CE MDR Registry: EUDAMEDGUDID Class:II
  • Listed Registry: GUDID Class:II
  • Oto Wizzard Ref K981511

    Active Regimes: 510(k) Registry: 510(k) Class:II

Rows 1-13 of 13

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
US-MF-000025226
FDA FEI number
1000307595
DUNS number
849311261
EU VAT number
59-3239914
EUDAMED status
Active
EUDAMED registered name
MedRx, Inc.
Registered address
1200, Starkey Road Suite 105, 33771, Largo, United States
Phone
+1888-392-1234
PRRC contact
Eddie Alford(public in EUDAMED)

EUDAMED certificates1

1 certificate1 valid, 0 expiredMDR 1next expiry 8 May 2028

EUDAMED certificates (1)

TÜV SÜD Product Service GmbH 0123 1 certificate

  • G10 101355 0009 Active

    Quality management system EU MDR

    Issued
    9 May 2023
    Expires
    8 May 2028

Frequently asked questions

How many devices does Medrx, Inc. have in the registry?

The registry currently lists 13 devices for Medrx, Inc.. Devices recorded under merged duplicate company entries are counted once.

Which registries list Medrx, Inc.'s devices?

Among its 13 most recently registered devices, Medrx, Inc. has devices listed in EUDAMED (8 devices), FDA 510(k) (1 device) and FDA GUDID (12 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do Medrx, Inc.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for Medrx, Inc.'s devices are Class I and Class II. Each device page shows its own class and authorisation.

What EUDAMED certificates are recorded for Medrx, Inc.?

EUDAMED lists 1 certificate for Medrx, Inc. (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 9 May 2023.

What are the newest devices from Medrx, Inc. in the registry?

The most recently registered devices listed for Medrx, Inc. include MedRx Avant HIT+, MedRx Video Otoscope, MedRx Avant REMsp and MedRx Avant A2D+.

Generated automatically from registry data and not verified by a human reviewer.