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Insight

FDA UDI

Class I (US FDA UDI)

by Marketlab Inc.

Identity

Trade Name
Insight FDA UDI
Generic Name
Examination/operating table component trolley FDA UDI
Device Name
Insight GynoCart Exam Cart FDA UDI
Model / Reference
138016 FDA UDI
Description
Insight GynoCart Exam Cart FDA UDI

Identifiers

Primary DI / UDI-DI
00817517026894 FDA UDI
FDA Product Code
LGX FDA UDI
GMDN Term
Examination/operating table component trolley FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4960 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Examination/operating table component trolley

Insight by Marketlab Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Examination/operating table component trolley.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Marketlab Inc.

Sources (1)

  • FDA UDI ae5dc408-0c0a-41bc-a155-26512e676746 33 fields · synced Jun 6, 2026