← Back to catalogue

MINOP® InVent

EUDAMEDFDA UDI

Class I (EU MDR)

Ref RT068R

by Aesculap AG

Identity

Trade Name
MINOP® InVent EUDAMED
MINOP FDA UDI
Generic Name
Surgical retraction system mounting frame, reusable FDA UDI
Device Name
MINOP INVENT adapter for holding arm EUDAMEDFDA UDI
Model / Reference
RT068R EUDAMEDFDA UDI
Description
MINOP INVENT ADAPTER FOR HOLDING ARM FDA UDI

Identifiers

Catalog Number
RT068R FDA UDI
Primary DI / UDI-DI
04046963832803 EUDAMEDFDA UDI
Basic UDI-DI
403923900000122826 EUDAMED
Direct Marketing DI
04046963832803 EUDAMED
FDA Product Code
GAD FDA UDI
EMDN Code
Z12029080 VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI-INVASIVE SURGERY - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Surgical retraction system mounting frame, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 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

MINOP® InVent 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Aesculap AG
EUDAMED SRN
DE-MF-000005504

Sources (2)

  • EUDAMED 638acc81-f303-4088-93ea-dd56f994f2fe 61 fields · synced Jul 9, 2026
  • FDA UDI 44c75d18-197d-4448-8966-229f99a593c5 35 fields · synced May 29, 2026