← Back to catalogue

Aico

FDA UDI

Class I (US FDA UDI)

by Arias International Company

Identity

Trade Name
AICO FDA UDI
Generic Name
Orthodontic pliers FDA UDI
Device Name
DISTAL END CUTTER UN FDA UDI
Model / Reference
7604901S FDA UDI
Description
DISTAL END CUTTER UN FDA UDI

Identifiers

Catalog Number
7604901S FDA UDI
Primary DI / UDI-DI
D1347604901S0 FDA UDI
FDA Product Code
EJY FDA UDI
GMDN Term
Orthodontic pliers 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

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

Category: Orthodontic pliers

Aico by Arias International Company — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthodontic pliers.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Sources (1)

  • FDA UDI 42a296dc-b5be-427f-add0-cf8b2202f969 34 fields · synced May 30, 2026