← Back to catalogue

Henry Schein Maxima

EUDAMED

Class I (EU MDR)

Ref 9000753Model TF-230 (HSM)

by Henry Schein Inc.

Identity

Trade Name
Henry Schein Maxima EUDAMED
Device Name
Mouth mirrors EUDAMED
Model / Reference
TF-230 (HSM) EUDAMED
9000753 EUDAMED

Identifiers

Primary DI / UDI-DI
10304040025342 EUDAMED
Basic UDI-DI
03040423001BC EUDAMED
Unit of Use DI
00304040025345 EUDAMED
EMDN Code
L160201 DENTAL MIRRORS AND HANDLES, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Henry Schein Maxima by Henry Schein, 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Henry Schein Inc.
EUDAMED SRN
US-MF-000021683
Authorised Representative
Henry Schein Services GmbH DE-AR-000008001

Sources (1)

  • EUDAMED 3e4f8ec2-14ce-45c6-bf91-7b8f221d09d9 61 fields · synced May 22, 2026