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American Eagle Instruments

FDA UDI

Class I (US FDA UDI)

by American Eagle Instruments

Identity

Trade Name
American Eagle Instruments FDA UDI
Generic Name
Instrument tray, reusable FDA UDI
Device Name
CASSETTE MCG. SURGICAL FDA UDI
Model / Reference
MCGSURG FDA UDI
Description
CASSETTE MCG. SURGICAL FDA UDI

Identifiers

Catalog Number
MCGSURG FDA UDI
Primary DI / UDI-DI
00841013115684 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
Instrument tray, reusable 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

American Eagle Instruments by American Eagle Instruments — 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

Sources (1)

  • FDA UDI cf134f02-8cb0-4b4b-86c3-d5409e9bdde1 36 fields · synced Jun 9, 2026