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Amnotec

FDA UDI

Class II (US FDA UDI)

by AMNOTEC International Medical GmbH

Identity

Trade Name
AMNOTEC FDA UDI
Generic Name
Rigid optical laparoscope FDA UDI
Device Name
VEQTRON 4K UHD Laparoscope, Ø 5.5 mm, 30°, WL. 310 mm, Autoclavable FDA UDI
Model / Reference
72-405-30 NIR FDA UDI
Description
VEQTRON 4K UHD Laparoscope, Ø 5.5 mm, 30°, WL. 310 mm, Autoclavable FDA UDI

Identifiers

Catalog Number
72-405-30 NIR FDA UDI
Primary DI / UDI-DI
04250942104533 FDA UDI
FDA Product Code
GCJ FDA UDI
GMDN Term
Rigid optical laparoscope 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

Yes

FDA UDI
Sterilization Method
Dry Heat Sterilization FDA UDI

Category: Rigid optical laparoscope

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

Similar devices

Also classified as Rigid optical laparoscope.

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 405513af-365b-406f-b8cd-58846c632a42 34 fields · synced May 30, 2026