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CamNtech Ltd

Active in EUDAMED
Also registered as CAMNTECH

United Kingdomfrom SRN EUDAMED FDA SRN GB-MF-000004683

CamNtech Ltd is a medical device manufacturer based in the United Kingdom, with 7 devices listed in EUDAMED, FDA GUDID and FDA 510(k) (EU Class I; FDA Class II) as of 14 Nov 2026.

Devices
7
Registrations
EUDAMEDFDA
FDA recalls
0

Registry facts

Counted by deviCERTS from registry records, 14 Nov 2026

Registries
  • EUDAMED 5
  • FDA GUDID 4
  • FDA 510(k) 2

A device listed in two registries counts in both.

Device classes
  • EU Class I 5
  • FDA Class II 2
Sites and related companies
Identifiers
  • EUDAMED SRN GB-MF-000004683

At a glance

Counted by deviCERTS from registry records

Market reach

European Union
EUDAMED actor
United States
FDA establishment
Authorised rep.
QbD RepS BVBE

Catalogue7

Newest first, rows 1-7 of 7

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
GB-MF-000004683
EUDAMED status
Active
EUDAMED registered name
CamNtech Ltd
Registered address
Manor Farm, Riband House, PE289JD, Fenstanton, United Kingdom (ex Northern Ireland)
PRRC contact
Howard Smith(public in EUDAMED)

FDA establishments1

Registered with the FDA under this company group, matched by name.

  • Camntech Limited US

Frequently asked questions

How many devices does CamNtech Ltd have in the registry?

The registry currently lists 7 devices for CamNtech Ltd. Devices recorded under merged duplicate company entries are counted once.

Which registries list CamNtech Ltd's devices?

Among its 7 most recently registered devices, CamNtech 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 CamNtech Ltd's devices fall under?

Among its 7 most recently registered devices, the classes recorded for CamNtech Ltd's devices are Class I and Class II. Each device page shows its own class and authorisation.

What are the newest devices from CamNtech Ltd in the registry?

The most recently registered devices listed for CamNtech Ltd include MOTION WATCH AND PRO-DIARY, ACTIWAVE 1E, ACTIWAVE2E, ACTIWAVE2M, ACTIWAVE4E, ACTIWAVE CARDIO MODEL 08-514, 08-521, 08-536, 08-557, 08-603, MotionWatch R and MotionWatch 8.

Which FDA establishments are linked to CamNtech Ltd?

1 FDA establishment is linked to CamNtech Ltd in the registry; they are listed on the company page.

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