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LockeT

EUDAMED

Class I (EU MDR)

Ref 9301

by Catheter Precision, Inc

Identity

Trade Name
LockeT EUDAMED
Device Name
LockeT Suture Retention Device EUDAMED
Model / Reference
9301 EUDAMED

Identifiers

Primary DI / UDI-DI
00851424007157 EUDAMED
Basic UDI-DI
08514240079301HW EUDAMED
EMDN Code
H9099 SUTURE DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

LockeT by Catheter Precision, Inc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000018898
Authorised Representative
MedNet EC-REP GmbH DE-AR-000000002

Sources (1)

  • EUDAMED 7841c3d6-b218-4cfe-9bcf-62f5c5997900 61 fields · synced Jun 18, 2026