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MIS Blade Illuminator - 4mm Max Cable Diameter

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 698.605S

by Lumitex Medical Devices, Inc.

Identity

Trade Name
Globus Medical MIS Blade Illuminator FDA UDI
Generic Name
Surgical instrument fibreoptic light FDA UDI
Device Name
MIS Blade Illuminator - 4mm Max Cable Diameter EUDAMED
Model / Reference
698.605S EUDAMED
009606 FDA UDI

Identifiers

Catalog Number
698.605S FDA UDI
Primary DI / UDI-DI
00812432021450 EUDAMEDFDA UDI
Basic UDI-DI
B-00812432021450 EUDAMED
FDA Product Code
FDG FDA UDI
EMDN Code
V9012 NON-SPECIALIST SURGICAL INSTRUMENTS AND KITS, SINGLE-USE EUDAMED
GMDN Term
Surgical instrument fibreoptic light FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class I FDA UDI
Regulation Number
876.4530 FDA UDI
Market of Registration
Netherlands 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

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

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

MIS Blade Illuminator - 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 cdddf6ad-7892-45b5-b61a-827b76473dea 61 fields · synced Jul 22, 2026
  • FDA UDI 39168a14-3f2f-4f36-8142-f9f609b459bb 33 fields · synced May 30, 2026