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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
Rigid optical mediastinoscope FDA UDI
Device Name
Distending Video Mediastinoscope FDA UDI
Model / Reference
10972SP FDA UDI
Description
Distending Video Mediastinoscope FDA UDI

Identifiers

Primary DI / UDI-DI
04048551242889 FDA UDI
FDA Product Code
EWY FDA UDI
GMDN Term
Rigid optical mediastinoscope FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.4720 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Rigid optical mediastinoscope

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

Similar devices

Also classified as Rigid optical mediastinoscope.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI 8b0f804f-e72a-4a22-8e57-15e5a2be8540 33 fields · synced Jun 1, 2026