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Tessa

by Surgical Dynamics Ltd 7 variants

Ref NF04R, NF09R, NF02R, NF03R, NF07R, NF01RModel FORCEPS

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number506056849TFORCEPSRVA Basic UDI-DI Date26 Mar 2026RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Forceps
Reusable Retractors
Model / Reference
FORCEPS, NF04R, NF09R, NF02R, NF03R, NF07R, NF01R
Primary DI / UDI-DI
05060568490717, 05060568490762, 05060568490694, 05060568490700, 05060568490748, 05060568490687
Basic UDI-DI
506056849TFORCEPSRVA, 506056849RETRACTORSRLH
EMDN Code
L03130401, L03140199
Device Class
Class I
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
UK-MF-000047364
Authorised representative
Advena Limited MT-AR-000000234

Other devices from Surgical Dynamics Ltd

Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No