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Endo Carver Glick 1

EUDAMEDFDA UDI

Class I (EU MDR)

Ref AEEMG1CA

by American Eagle Instruments

Identity

Trade Name
ENDO CARVER GLICK 1 EUDAMED
American Eagle Instruments FDA UDI
Generic Name
Dental restoration carver, amalgam, reusable FDA UDI
Device Name
Carvers, Discoids, Margin Trimmers EUDAMED
ENDO CARVER GLICK 1 FDA UDI
Model / Reference
AEEMG1CA EUDAMEDFDA UDI
Description
ENDO CARVER GLICK 1 FDA UDI

Identifiers

Catalog Number
AEEMG1CA FDA UDI
Primary DI / UDI-DI
00841013104749 EUDAMEDFDA UDI
Basic UDI-DI
0841013135793EKHA737881JJ EUDAMED
FDA Product Code
EKH FDA UDI
EMDN Code
Q01010199 DENTAL RESTORATION DEVICES - OTHER EUDAMED
GMDN Term
Dental restoration carver, amalgam, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.4565 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

Yes

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

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental appliance fabrication material, ceramic

Endo Carver Glick 1 by American Eagle Instruments — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental appliance fabrication material, ceramic.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000018222
Authorised Representative
Young Microbrush Ireland Ltd IE-AR-000011249

Sources (2)

  • EUDAMED 5cd30549-af38-4259-aa3d-652850fb780e 61 fields · synced Jun 19, 2026
  • FDA UDI 4ac437fd-cd0a-4c3f-9a86-f6929f3ce120 35 fields · synced May 30, 2026