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Karl Storz Scb

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
KARL STORZ SCB FDA UDI
Generic Name
Operating room audiovisual data/device management system FDA UDI
Device Name
KARL STORZ OR1 control FDA UDI
Model / Reference
20097020-1 FDA UDI
Description
KARL STORZ OR1 control FDA UDI

Identifiers

Primary DI / UDI-DI
04048551062265 FDA UDI
FDA Product Code
ODA FDA UDI
GMDN Term
Operating room audiovisual data/device management system 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

No

FDA UDI

Category: Operating room audiovisual data/device management system

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

Similar devices

Also classified as Operating room audiovisual data/device management system.

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 bccd825b-6252-46b2-ab5a-92adef67200d 33 fields · synced May 30, 2026