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Nordent Manufacturing, Inc.

EUDAMED

Class I (EU MDR)

Ref Nordent Catalogue Surgical SectionModel REPGF14

by Nordent Manufacturing Inc.

Identity

Trade Name
Nordent Manufacturing, Inc. EUDAMED
Device Name
PERIOSTEAL ELEVATOR DE G/FOX 14, MEDIUM ROUND HANDLE EUDAMED
Model / Reference
REPGF14 EUDAMED
Nordent Catalogue Surgical Section EUDAMED

Identifiers

Primary DI / UDI-DI
00840018658615 EUDAMED
Basic UDI-DI
0840018686156N EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Surgical retraction system, reusable

Nordent Manufacturing, Inc. by Nordent Manufacturing Inc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000048439
Authorised Representative
Ukens Dental DE-AR-000022084

Sources (1)

  • EUDAMED 65aeaa14-7825-495a-93aa-e6e4ff62d7dd 61 fields · synced May 22, 2026