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HM Fräser

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 0710.023HPModel 17761

by Edenta Etablissement

Identity

Trade Name
HM Fräser EUDAMED
EDENTA FDA UDI
Generic Name
Carbide dental bur, reusable FDA UDI
Device Name
Podologie Schleifer EUDAMED
TC Cutter FDA UDI
Model / Reference
17761 EUDAMED
0710.023HP EUDAMEDFDA UDI
Description
TC Cutter FDA UDI

Identifiers

Catalog Number
UC138E-023 FDA UDI
Primary DI / UDI-DI
E3120710023HP1 EUDAMEDFDA UDI
Basic UDI-DI
++E31217761EX EUDAMED
FDA Product Code
EJL FDA UDI
EMDN Code
Z12110102 DENTAL DRILLS EUDAMED
GMDN Term
Carbide dental bur, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.3240 FDA UDI
Market of Registration
Liechtenstein EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

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

No

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

Yes

FDA UDI

HM Fräser by Edenta Etablissement — Class IIa — 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

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Manufacturer

EUDAMED SRN
LI-MF-000011937

Sources (2)

  • EUDAMED a2e659c4-9c74-46ba-bd08-bc1b5abeb6d1 61 fields · synced Sep 17, 2026
  • FDA UDI 681d3c9a-9764-41f1-8f6f-ff3f3ffbe430 34 fields · synced May 30, 2026