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Mobile ENT Computer Cart, Assembly

FDA UDI

Class II (US FDA UDI)

by Neurologica Corporation

Identity

Trade Name
Mobile ENT Computer Cart, Assembly FDA UDI
Generic Name
CT system workstation FDA UDI
Model / Reference
10-00159-001 FDA UDI

Identifiers

Primary DI / UDI-DI
10815411020212 FDA UDI
FDA Product Code
JAK FDA UDI
GMDN Term
CT system workstation FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.1750 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: CT system workstation

Mobile ENT Computer Cart, Assembly by Neurologica Corporation — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as CT system workstation.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI c50c7b91-71db-49c6-abd4-47df6f9a96e7 32 fields · synced Jun 8, 2026