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ITS Model-L

FDA UDI

Class II (US FDA UDI)

by InTheSmart Co., Ltd.

Identity

Trade Name
ITS Model-L FDA UDI
Generic Name
Endoscopic light source unit, line-powered FDA UDI
Model / Reference
ITSEL1711 FDA UDI

Identifiers

Primary DI / UDI-DI
08800033200024 FDA UDI
FDA Product Code
FCQ FDA UDI
GMDN Term
Endoscopic light source unit, line-powered 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

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endoscopic light source unit, line-powered

ITS Model-L by InTheSmart Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endoscopic light source unit, line-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 21c5f491-c953-4a99-83bb-0a98f7506ca7 32 fields · synced May 29, 2026