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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
Orthodontic pliers FDA UDI
Device Name
DR. ALLEN KIT FDA UDI
Model / Reference
AEALLKIT FDA UDI
Description
DR. ALLEN KIT FDA UDI

Identifiers

Catalog Number
AEALLKIT FDA UDI
Primary DI / UDI-DI
00841013101847 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Orthodontic pliers FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

Yes

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 d9d79766-8ae0-4a3d-9e3c-feb6f94bca73 36 fields · synced Jun 9, 2026