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Dornier MedTech

FDA UDI

Class II (US FDA UDI)

by Dornier MedTech America, Inc.

Identity

Trade Name
Dornier MedTech FDA UDI
Generic Name
Endoscopic video image processing unit FDA UDI
Device Name
Digital Video Processor, Input Voltage: 5V 2A (for use with Dornier Ureteroscope) FDA UDI
Model / Reference
Axis Video Processor FDA UDI
Description
Digital Video Processor, Input Voltage: 5V 2A (for use with Dornier Ureteroscope) FDA UDI

Identifiers

Catalog Number
AXPEOSB FDA UDI
Primary DI / UDI-DI
00810116020713 FDA UDI
FDA Product Code
FGB FDA UDI
GMDN Term
Endoscopic video image processing unit 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic video image processing unit

Dornier MedTech by Dornier MedTech America, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic video image processing unit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 86d28f0c-3a5b-4523-abf4-343738b270e4 34 fields · synced Jun 9, 2026