← Back to catalogue

Oktagon

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 93721Model Accessories for prothetic parts

by Hager & Meisinger GmbH

Identity

Trade Name
Oktagon EUDAMED
OKTAGON® FDA UDI
Generic Name
Manual non-rotary dental instrument handle FDA UDI
Device Name
Device for prosthetic application (impression, laboratory) FDA UDI
Model / Reference
Accessories for prothetic parts EUDAMED
93721 EUDAMEDFDA UDI
Description
Device for prosthetic application (impression, laboratory) FDA UDI

Identifiers

Catalog Number
93721 FDA UDI
Primary DI / UDI-DI
E0HM937211 EUDAMEDFDA UDI
Basic UDI-DI
++E0HM311I01AAM9 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010280 PROSTHETIC DENTISTRY DEVICES - ACCESSORIES EUDAMED
GMDN Term
Manual non-rotary dental instrument handle FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Oktagon by Hager & Meisinger GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
DE-MF-000004966

Sources (2)

  • EUDAMED 1b5d242f-ca06-4a50-8e6a-459ae3a475e8 61 fields · synced Oct 5, 2026
  • FDA UDI 23c26f16-0a18-4b1d-b65e-cac3a10b5311 35 fields · synced May 30, 2026