← Back to catalogue

Karl Storz Aida

FDA UDI

Class II (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name
KARL STORZ AIDA FDA UDI
Generic Name
Operating room audiovisual data/device management system FDA UDI
Device Name
AIDA DVD-M HD Kit, DOMESTIC, CE FDA UDI
Model / Reference
20200075U FDA UDI
Description
AIDA DVD-M HD Kit, DOMESTIC, CE FDA UDI

Identifiers

Primary DI / UDI-DI
04048551356388 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Operating room audiovisual data/device management system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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 Aida 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

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

Manufacturer

Manufacturer
Karl Storz GmbH & Co. KG

Sources (1)

  • FDA UDI d1bc9b45-3bcc-4eec-a6ee-90e983514042 33 fields · synced Jun 8, 2026