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Dci

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
DCI FDA UDI
Generic Name
Fibreoptic light cable FDA UDI
Device Name
DCI®Fiber Optic Light Cable,320cm,Ø2.5mm FDA UDI
Model / Reference
495DV FDA UDI
Description
DCI®Fiber Optic Light Cable,320cm,Ø2.5mm FDA UDI

Identifiers

Primary DI / UDI-DI
04048551168561 FDA UDI
FDA Product Code
FCW FDA UDI
GMDN Term
Fibreoptic light cable 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Fibreoptic light cable

Dci by Karl Storz GmbH & Co. KG — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic light cable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1bac398a-02de-4a14-ba3c-d2b4a7398a69 33 fields · synced Jun 1, 2026