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EleVision™

FDA UDI

Class II (US FDA UDI)

by SCHÖLLY FIBEROPTIC GmbH

Identity

Trade Name
EleVision™ FDA UDI
Generic Name
Endoscope video camera FDA UDI
Device Name
EleVision TM 4K Camera Head FDA UDI
Model / Reference
ELEV4KCAM FDA UDI
Description
EleVision TM 4K Camera Head FDA UDI

Identifiers

Primary DI / UDI-DI
04250480113639 FDA UDI
FDA Product Code
GCJ FDA UDI
FET FDA UDI
OWN FDA UDI
GMDN Term
Endoscope video camera FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
876.1500 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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

No

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

Category: Endoscope video camera

EleVision™ by SCHÖLLY FIBEROPTIC GmbH — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscope video camera.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f1480ebf-d27b-4517-b780-a96849de2cfb 35 fields · synced May 30, 2026