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Galaxy II LUX Connect - 4mm Max Cable Diameter

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref JUNELuxC1

by Lumitex Medical Devices, Inc.

Identity

Trade Name
June Medical Galaxy II LUX Connect Surgical Illuminator FDA UDI
Generic Name
Open surgical site internal light FDA UDI
Device Name
Galaxy II LUX Connect - 4mm Max Cable Diameter EUDAMED
Model / Reference
JUNELuxC1 EUDAMED
012569 FDA UDI

Identifiers

Catalog Number
JUNELuxC1 FDA UDI
Primary DI / UDI-DI
00812432022471 EUDAMEDFDA UDI
Basic UDI-DI
B-00812432022471 EUDAMED
FDA Product Code
FDG FDA UDI
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED
GMDN Term
Open surgical site internal light FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
876.4530 FDA UDI
Market of Registration
Sweden EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Surgical retractor/retraction system blade, single-use

Galaxy II LUX Connect - 4mm Max Cable Diameter by Lumitex Medical Devices, Inc. — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID

Similar devices

Also classified as Surgical retractor/retraction system blade, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
US-MF-000030520
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (2)

  • EUDAMED 00eb606f-bfbc-4158-a516-7aa5e50d56ff 61 fields · synced Jul 23, 2026
  • FDA UDI 40602910-94cc-48e1-8708-2f3917ca7edd 33 fields · synced May 29, 2026