Tessa

by Surgical Dynamics Ltd 7 variants

Ref NF06RModel 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

Region	Authorization	Number	Date	Status
European Union	CE/MDR	Number506056849TFORCEPSRVA Basic UDI-DI 05060568490731UDI-DI	Date26 Mar 2026Registered	StatusActive

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

Active
Expiring
Withdrawn
Listed
Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name: Forceps
Model / Reference: FORCEPS, NF06R

Primary DI / UDI-DI: 05060568490731
Basic UDI-DI: 506056849TFORCEPSRVA
EMDN Code: L03130401 Tissue and organ grasping forceps, reusable

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

Tessa

Class I
Tessa

Class I
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Class I
Tessa

Class I
Tessa

Class I
Tessa

Class I

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