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Offset Reamer Handle - Instrument Tray

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 50740102Model 50740101

by Incipio Devices SA

Identity

Trade Name
Offset Reamer Handle - Instrument Tray EUDAMEDFDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
Cup Instrument System - Instrument Tray EUDAMED
Surgical instrument tray for Incipio Devices offset reamer handle FDA UDI
Model / Reference
50740101 EUDAMED
50740102 EUDAMEDFDA UDI
Description
Surgical instrument tray for Incipio Devices offset reamer handle FDA UDI

Identifiers

Catalog Number
50740102 FDA UDI
Primary DI / UDI-DI
07630055303219 EUDAMEDFDA UDI
Basic UDI-DI
76300553507401INTFU EUDAMED
Direct Marketing DI
07630055303219 EUDAMED
FDA Product Code
FSM FDA UDI
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED
GMDN Term
Instrument tray, reusable FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
878.4800 FDA UDI
Market of Registration
Austria 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical retraction system, reusable

Offset Reamer Handle - Instrument Tray by Incipio Devices SA — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Incipio Devices SA
EUDAMED SRN
CH-MF-000030518
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED ce381075-789c-46da-9a86-38998c96da7e 61 fields · synced Jun 20, 2026
  • FDA UDI 176cfeea-4ccb-4470-9b68-94753fbc5198 34 fields · synced May 30, 2026