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Amnotec

FDA UDI

Class I (US FDA UDI)

by AMNOTEC International Medical GmbH

Identity

Trade Name
AMNOTEC FDA UDI
Generic Name
Electromechanical device/system transport trolley FDA UDI
Device Name
Swivel Arm, Single, for Second TFT- Monitor, Max. load: 3 - 10 kg FDA UDI
Model / Reference
71-705-46 FDA UDI
Description
Swivel Arm, Single, for Second TFT- Monitor, Max. load: 3 - 10 kg FDA UDI

Identifiers

Catalog Number
71-705-46 FDA UDI
Primary DI / UDI-DI
04056634016593 FDA UDI
FDA Product Code
BZN FDA UDI
GMDN Term
Electromechanical device/system transport trolley FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.6175 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electromechanical device/system transport trolley

Amnotec by AMNOTEC International Medical GmbH — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electromechanical device/system transport trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
AMNOTEC International Medical GmbH

Sources (1)

  • FDA UDI 18eeedfc-42bb-46e7-bfc5-9520ae604397 34 fields · synced May 30, 2026