← Back to catalogue

Al-7000x

EUDAMEDFDA UDI

Class I (EU MDR)

Ref AL-7000XModel Light Guide Adapters

by Schölly Fiberoptic Gmbh

Identity

Trade Name
NA FDA UDI
Generic Name
Light source adaptor FDA UDI
Device Name
Light Guide Adapter AL-7000X FDA UDI
Model / Reference
Light Guide Adapters EUDAMED
AL-7000X EUDAMEDFDA UDI
Description
Light Guide Adapter AL-7000X FDA UDI

Identifiers

Primary DI / UDI-DI
04250480101735 EUDAMEDFDA UDI
Basic UDI-DI
42504801LGADAPTERSFQ EUDAMED
Direct Marketing DI
04250480101735 EUDAMED
FDA Product Code
NTN FDA UDI
EMDN Code
Z12020480 INSTRUMENTS FOR THE ACQUISITION AND MANAGEMENT OF ENDOSCOPIC AND MINIMALLY INVASIVE SURGERY IMAGES - HARDWARE ACCESSORIES EUDAMED
GMDN Term
Light source adaptor 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Al-7000x by SCHÖLLY FIBEROPTIC GmbH — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000005618

Sources (2)

  • EUDAMED 7b6924fd-bf64-4ba9-bf76-d10dc2804244 61 fields · synced Aug 1, 2026
  • FDA UDI c739bdd9-3ab4-4fb1-b501-1e40535fc85a 35 fields · synced May 30, 2026