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miniARM™

FDA UDI

Class I (US FDA UDI)

by LSI Solutions, Inc.

Identity

Trade Name
miniARM™ FDA UDI
Generic Name
Surgical instrument assist arm system, manually-adjusted FDA UDI
Device Name
miniARM™ INSTRUMENT HOLDER LEFT FDA UDI
Model / Reference
080418 FDA UDI
Description
miniARM™ INSTRUMENT HOLDER LEFT FDA UDI

Identifiers

Catalog Number
080418 FDA UDI
Primary DI / UDI-DI
00850200006858 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Surgical instrument assist arm system, manually-adjusted FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Length — 30 Centimeter FDA UDI

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

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 d4451d2b-b0d3-4efa-8dc6-f7552b9745e2 37 fields · synced May 30, 2026