Pricing Sign in

Role
Country
Date of registration
Address

Made In Tracker

Made In Tracker EasyUDI

Legal

Privacy Policy Legal Notice

About

About FAQ Contact

Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

Subscribe to our monthly newsletter:

By subscribing, you accept the General Personal Data Protection Policy.

Organization name
UDI-DI code
Reference / catalog number

LG-7000X — Class I MDR by SCHÖLLY FIBEROPTIC GMBH

MD Atlas
SCHÖLLY FIBEROPTIC GMBH

EUDAMED last updated this device on Apr 14, 2026

LG-7000X

42504801FOLIGHTGUIDESHV

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: SCHÖLLY FIBEROPTIC GMBH
UDI-DI code: 04250480104118
Reference / catalog number: LG-7000X

Sign in to open the EUDAMED record

The link to the official EUDAMED page is reserved for signed-in users. Create a free account to continue.

Email

Password

No account yet?

Manufacturer information

Organization name: SCHÖLLY FIBEROPTIC GMBH
SRN: DE-MF-000005618
Manufacturer status: Active

Related devices

AlphaScope42504801LAPAROSCOPESEFOn the market AlphaScope42504801LAPAROSCOPESEFOn the market BULKAMID ®42504801CYSTOSCOPES7FOn the market UROLIFT ®42504801CYSTOSCOPES7FOn the market UROLIFT ®42504801CYSTOSCOPES7FOn the market

Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 2 countries total.

Country	On market since	Until
GermanyPrimary placement		Still on market
Türkiye		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04250480104118
Basic UDI-DI: 42504801FOLIGHTGUIDESHV
Reference / catalog number: LG-7000X
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: https://www.schoelly.de/en/instructions-for-use-1
Clinical sizes: 3.5 MU50
3000 MU50

EMDN nomenclature code(s)

Z12020480INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification