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Ergoprobe

EUDAMEDFDA UDI

Class I (EU MDR)

Ref DA083

by Aesculap AG

Identity

Trade Name
ERGOPROBE EUDAMEDFDA UDI
Generic Name
Dental mirror, reusable FDA UDI
Device Name
Mouth mirror EUDAMED
ERGOPROBE MOUTH MIRROR HANDLE BLACK FDA UDI
Model / Reference
DA083 EUDAMEDFDA UDI
Description
ERGOPROBE MOUTH MIRROR HANDLE BLACK FDA UDI

Identifiers

Catalog Number
DA083 FDA UDI
Primary DI / UDI-DI
04046964540066 EUDAMEDFDA UDI
Basic UDI-DI
4039239000000512ZU EUDAMED
Direct Marketing DI
04046964540066 EUDAMED
FDA Product Code
EAX FDA UDI
EMDN Code
L160201 DENTAL MIRRORS AND HANDLES, REUSABLE EUDAMED
GMDN Term
Dental mirror, 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

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

Ergoprobe by Aesculap AG — 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

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Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED 61594188-572e-4790-b5ea-a0c6e530b136 61 fields · synced Jul 13, 2026
  • FDA UDI 07aa6fa0-909c-487a-950f-1dae931dea34 35 fields · synced May 30, 2026