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Simple Solutions Medical

FDA UDI

Class I (US FDA UDI)

by Simple Solutions Medical

Identity

Trade Name
Simple Solutions Medical FDA UDI
Generic Name
Endobronchial tube FDA UDI
Device Name
Lung Isolation (Emergency Airway) Convenience Kit - Right - 35 Fr FDA UDI
Model / Reference
LIT-35-R FDA UDI
Description
Lung Isolation (Emergency Airway) Convenience Kit - Right - 35 Fr FDA UDI

Identifiers

Primary DI / UDI-DI
00860012609338 FDA UDI
FDA Product Code
OFP FDA UDI
GMDN Term
Endobronchial tube FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
868.5240 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Endobronchial tube

Simple Solutions Medical by Simple Solutions Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endobronchial tube.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI df8f5b09-c919-421f-a603-766ff99baedd 33 fields · synced May 30, 2026