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Wurzelkanal-Erweiterer "Gates" Sortiment

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 180.15.204SOModel 16411

by Edenta Etablissement

Identity

Trade Name
Wurzelkanal-Erweiterer "Gates" Sortiment EUDAMED
EDENTA FDA UDI
Generic Name
Endodontic enlarger, reusable FDA UDI
Device Name
Endo-Instrumente EUDAMED
Root canal reamers "Gates" FDA UDI
Model / Reference
16411 EUDAMED
180.15.204SO EUDAMEDFDA UDI
Description
Root canal reamers "Gates" FDA UDI

Identifiers

Catalog Number
EG204-ASST FDA UDI
Primary DI / UDI-DI
E31218015204SO1 EUDAMEDFDA UDI
Basic UDI-DI
++E31216411DS EUDAMED
FDA Product Code
DZA FDA UDI
EMDN Code
L159004 ENDODONTIC RASPS AND FILES, REUSABLE EUDAMED
GMDN Term
Endodontic enlarger, reusable FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
872.4130 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

Yes

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Manual endodontic file/rasp, reusable

Wurzelkanal-Erweiterer "Gates" Sortiment by Edenta Etablissement — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Manual endodontic file/rasp, reusable.

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 2bec1453-a126-4061-b4fd-aacc3a00f1dd 61 fields · synced Jul 21, 2026
  • FDA UDI 0686f52c-302a-4dff-8547-4e95ab10c613 34 fields · synced May 30, 2026