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CamDiab

Active in EUDAMED

United Kingdomfrom SRN EUDAMED SRN GB-MF-000001893

CamDiab is a medical device manufacturer based in the United Kingdom, with 7 devices listed in EUDAMED and FDA 510(k) (EU Class III and IIb; FDA Class II) as of 13 Nov 2026.

Devices
7
Registrations
EUDAMED

Registry facts

Counted by deviCERTS from registry records, 13 Nov 2026

Registries
  • EUDAMED 5
  • FDA 510(k) 2

A device listed in two registries counts in both.

Device classes
  • EU Class III 4
  • FDA Class II 2
  • EU Class IIb 1
Sites and related companies
Identifiers
  • EUDAMED SRN GB-MF-000001893

At a glance

Counted by deviCERTS from registry records

EU certificates

2 of 2 in force.

See certificates

Market reach

European Union
EUDAMED actor, 2 certificates
Authorised rep.
CEpartner4UNL

Catalogue7

Newest first, rows 1-7 of 7

  • CamAPS FX Ref IFX0002

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • CamAPS HX Ref AHX0002

    Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:III
  • CamAPS FX Ref AFX0002

    Active Regimes: CE MDR Registry: EUDAMED Class:III
  • CamAPS HX Ref IHX0002

    Withdrawn Regimes: CE MDR, withdrawn Registry: EUDAMED Class:III
  • CamAPS FX Ref K232603

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • iOS CamAPS FX Ref K261896

    Active Regimes: 510(k) Registry: 510(k) Class:II
  • CamAPS FX Ref UK00003281765

    Active Regimes: CE MDD Registry: EUDAMED Class:IIb

Company details

EUDAMED record synced 7 Nov 2026

EUDAMED SRN
GB-MF-000001893
EU VAT number
GB333918003
EUDAMED status
Active
EUDAMED registered name
CamDiab
Registered address
Hills Road, CB2 0QQ, Cambridge, United Kingdom (ex Northern Ireland)
Phone
+44 203 695 3780
PRRC contact
Nicole Ashcroft(public in EUDAMED)

EUDAMED certificates2

2 certificates2 valid, 0 expiredMDR 2next expiry 13 Mar 2029

EUDAMED certificates (2)

BSI Group The Netherlands B.V. 2797 2 certificates

  • MDR 757281 Active Supplemented

    Technical documentation EU MDR

    Issued
    18 Jun 2026
    Expires
    13 Mar 2029
    Reason
    Change approved
  • MDR 757283 Active Supplemented

    Quality management system EU MDR

    Issued
    18 Jun 2026
    Expires
    13 Mar 2029
    Reason
    Change approved

Frequently asked questions

How many devices does CamDiab have in the registry?

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

Which registries list CamDiab's devices?

Among its 7 most recently registered devices, CamDiab has devices listed in EUDAMED (5 devices) and FDA 510(k) (2 devices). A device can be listed in more than one registry, so these counts overlap.

What risk classes do CamDiab's devices fall under?

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

What EUDAMED certificates are recorded for CamDiab?

EUDAMED lists 2 certificates for CamDiab (technical documentation; quality management system) under MDR. The most recent was issued on 18 Jun 2026.

What are the newest devices from CamDiab in the registry?

The most recently registered devices listed for CamDiab include CamAPS FX, CamAPS HX and iOS CamAPS FX.

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