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Kerr Endoring e-Foam

EUDAMED

Class I (EU MDR)

Ref 825-0050Model ERK-EX-S

by Jordco, Inc.

Identity

Trade Name
Kerr Endoring e-Foam EUDAMED
Device Name
ENDORING EUDAMED
Model / Reference
ERK-EX-S EUDAMED
825-0050 EUDAMED

Identifiers

Primary DI / UDI-DI
00195062019074 EUDAMED
Basic UDI-DI
00859611ENDORINGUU EUDAMED
EMDN Code
Q010507 ENDODONTIC INSTRUMENTS (CANAL ENLARGERS, FILES, RASPS, ETC.), SINGLE-USE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Malta EUDAMED

Clinical & Handling

Sterile

No

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

Kerr Endoring e-Foam by Jordco, 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

Manufacturer
Jordco, Inc.
EUDAMED SRN
US-MF-000021671
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED e6266f7d-2471-45b2-a819-8a46240a48c0 61 fields · synced Jul 14, 2026