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Gimmi

FDA UDIEUDAMED

Class II (US FDA UDI)

Ref T.8024.25

by Gimmi GmbH

Identity

Trade Name
ALPHAPORT EUDAMED
Gimmi FDA UDI
Generic Name
Endoscope sheath, reusable FDA UDI
Device Name
Trocar Systems & Accessories EUDAMED
ALPHAPORT / MULTIFUNCTION REDUCER FROM Ø 12.5 MM TO 5.5 MM FOR ALL TROCAR SLEEVES FDA UDI
Model / Reference
T.8024.25 EUDAMEDFDA UDI
Description
ALPHAPORT / MULTIFUNCTION REDUCER FROM Ø 12.5 MM TO 5.5 MM FOR ALL TROCAR SLEEVES FDA UDI

Identifiers

Catalog Number
T.8024.25 FDA UDI
Primary DI / UDI-DI
04049047638766 EUDAMEDFDA UDI
Basic UDI-DI
4049047LGA09BJA27DREGM EUDAMED
Direct Marketing DI
04049047638766 EUDAMED
FDA Product Code
GCJ FDA UDI
EMDN Code
L031280 SURGICAL TROCAR, REUSABLE - ACCESSORIES EUDAMED
GMDN Term
Endoscope sheath, reusable FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
876.1500 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

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: Endoscope sheath, reusable

Gimmi by Gimmi GmbH — Class II — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope sheath, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Gimmi GmbH

Sources (2)

  • FDA UDI 25a21061-4f1e-427a-9a00-a666c13d09fb 35 fields · synced Jul 16, 2026
  • EUDAMED 6ffe0daa-903f-4647-a050-37535f6499d3 61 fields · synced Jul 16, 2026