Digitimer, Ltd.
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Digitimer, Ltd. is a medical device manufacturer, with 7 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (FDA Class II; EU Class IIa) as of 13 Nov 2026.
- Devices
- 7
Registry facts
- Registries
- EUDAMED 5
- FDA GUDID 4
- FDA 510(k) 2
- Device classes
- FDA Class II 6
- EU Class IIa 1
- Top EMDN categories
- Sites and related companies
- Digitimer Ltd. United Kingdom
What Digitimer, Ltd. makes
Digitimer, Ltd. makes diagnostic peripheral nerve electrical stimulation systems and neurophysiologic monitoring systems, including constant current stimulators such as the DS7AP and DS7A models.
Catalogue
- Regimes: CE MDD Registry: EUDAMED
- Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID
- Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID
- Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID
- Regimes: CE MDD 510(k) Registry: EUDAMEDGUDID
Digitimer DS7AP Constant Current Stimulator Ref K172381
Regimes: 510(k) Registry: 510(k)- Regimes: 510(k) Registry: 510(k)
Sites
- Digitimer Ltd. GBFEI 3003631667 1 device
Frequently asked questions
How many devices does Digitimer, Ltd. have in the registry?
The registry currently lists 7 devices for Digitimer, Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Digitimer, Ltd.'s devices?
Among its 7 most recently registered devices, Digitimer, Ltd. has devices listed in EUDAMED (5 devices), FDA 510(k) (2 devices) and FDA GUDID (4 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Digitimer, Ltd.'s devices fall under?
Among its 7 most recently registered devices, the classes recorded for Digitimer, Ltd.'s devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What are the newest devices from Digitimer, Ltd. in the registry?
The most recently registered devices listed for Digitimer, Ltd. include Isolated Bipolar Constant Current Stimulator, Digitimer DS7AH, Digitimer DS7A and Digitimer DS7AP.