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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
Endodontic plugger FDA UDI
Device Name
CONDENSER/PLUGGER 2T (TANNER) FDA UDI
Model / Reference
AEC/P2T FDA UDI
Description
CONDENSER/PLUGGER 2T (TANNER) FDA UDI

Identifiers

Catalog Number
AEC/P2T FDA UDI
Primary DI / UDI-DI
00841013102226 FDA UDI
FDA Product Code
EKR FDA UDI
GMDN Term
Endodontic plugger FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Category: Endodontic plugger

American Eagle Instruments by American Eagle Instruments — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Endodontic plugger.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI d31c5133-6e3b-44ff-aafa-a35eac17ebc0 34 fields · synced Jun 9, 2026