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miniARM® multiSTATION™ System

FDA UDI

Class I (US FDA UDI)

by LSI Solutions, Inc.

Identity

Trade Name
miniARM® multiSTATION™ System FDA UDI
Generic Name
Pleuroscopic/mediastinoscopic access cannula, reusable FDA UDI
Device Name
miniARM® CANNULA ADAPTOR KIT FDA UDI
Model / Reference
080415 FDA UDI
Description
miniARM® CANNULA ADAPTOR KIT FDA UDI

Identifiers

Catalog Number
080415 FDA UDI
Primary DI / UDI-DI
00850200006599 FDA UDI
FDA Product Code
GEA FDA UDI
GMDN Term
Pleuroscopic/mediastinoscopic access cannula, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Pleuroscopic/mediastinoscopic access cannula, reusable

miniARM® multiSTATION™ System by LSI Solutions, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Pleuroscopic/mediastinoscopic access cannula, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
LSI Solutions, Inc.

Sources (1)

  • FDA UDI 9d4112cc-cf57-4613-923e-efa44c5b9017 35 fields · synced May 30, 2026