← Back to catalogue

Aesculap

EUDAMEDFDA UDI

Class I (EU MDR)

Ref OP293R

by Aesculap AG

Identity

Trade Name
Aesculap EUDAMEDFDA UDI
Generic Name
Rigid optical laryngopharyngoscope FDA UDI
Device Name
Operating laryngoscope EUDAMED
OPERATING LARYNGOSCOPEF/ADLTMED140MM FDA UDI
Model / Reference
OP293R EUDAMEDFDA UDI
Description
OPERATING LARYNGOSCOPEF/ADLTMED140MM FDA UDI

Identifiers

Catalog Number
OP293R FDA UDI
Primary DI / UDI-DI
04038653013814 EUDAMEDFDA UDI
Basic UDI-DI
40392390000012472A EUDAMED
Direct Marketing DI
04038653013814 EUDAMED
FDA Product Code
CCW FDA UDI
EMDN Code
Z12021003 LARYNGOSCOPES EUDAMED
GMDN Term
Rigid optical laryngopharyngoscope FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
868.5540 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

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

Category: Laryngoscope blade, reusable

Aesculap by Aesculap AG — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laryngoscope blade, reusable.

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

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED aa7b8c1f-dc72-47f1-ab15-c82cb26a1a3a 61 fields · synced Jul 28, 2026
  • FDA UDI 6fff6cef-fee0-4f77-b886-a6ed42a1bdda 35 fields · synced May 30, 2026