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Minop® Trend

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref FH611R

by Aesculap AG

Identity

Trade Name
MINOP® TREND EUDAMED
AESCULAP FDA UDI
Generic Name
ENT trocar blade FDA UDI
Device Name
MINOP TREND irrigation/suction instr. EUDAMED
MINOP TREND IRRIG.SUCT.SHEATH 30DG D6MM FDA UDI
Model / Reference
FH611R EUDAMEDFDA UDI
Description
MINOP TREND IRRIG.SUCT.SHEATH 30DG D6MM FDA UDI

Identifiers

Catalog Number
FH611R FDA UDI
Primary DI / UDI-DI
04046963313722 EUDAMEDFDA UDI
Basic UDI-DI
40392390000028903G EUDAMED
Direct Marketing DI
04046963313722 EUDAMED
FDA Product Code
GWG FDA UDI
EMDN Code
Z12019007 IRRIGATORS EUDAMED
GMDN Term
ENT trocar blade FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.1480 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

No

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: Endoscopic spray catheter, single-use

Minop® Trend by Aesculap AG — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic spray catheter, single-use.

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 02aff162-1a89-4151-a3f2-dd7a5f48a232 61 fields · synced Jun 17, 2026
  • FDA UDI b703d269-5ba2-4235-a0b9-0ca38fdb2ade 36 fields · synced May 29, 2026