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American Eagle Instruments

FDA UDI

Class II (US FDA UDI)

by American Eagle Instruments

Identity

Trade Name
American Eagle Instruments FDA UDI
Generic Name
Ultrasonic dental scaling/debridement system handpiece tip, periodontal FDA UDI
Device Name
MAGNETOSTRICTIVE #100-30K BLUE FDA UDI
Model / Reference
AEUS30-100 FDA UDI
Description
MAGNETOSTRICTIVE #100-30K BLUE FDA UDI

Identifiers

Primary DI / UDI-DI
00841013112850 FDA UDI
FDA Product Code
ELC FDA UDI
GMDN Term
Ultrasonic dental scaling/debridement system handpiece tip, periodontal FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.4850 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

American Eagle Instruments by American Eagle Instruments — Class II — 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 416eb680-8520-4231-bd52-a26c280618ef 34 fields · synced Jun 9, 2026