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Guide Pin

FDA UDI

Class I (US FDA UDI)

by Megagen Implant Co. Ltd

Identity

Trade Name
Guide Pin FDA UDI
Generic Name
Dental precision attachment simulator/analog, single-use FDA UDI
Device Name
ARi ExCon Implant System FDA UDI
Model / Reference
ARIEGPP25 FDA UDI
Description
ARi ExCon Implant System FDA UDI

Identifiers

Catalog Number
ARIEGPP25 FDA UDI
Primary DI / UDI-DI
08809854029210 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental precision attachment simulator/analog, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 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

Yes

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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental precision attachment simulator/analog, single-use

Guide Pin by Megagen Implant Co. Ltd — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental precision attachment simulator/analog, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Megagen Implant Co. Ltd

Sources (1)

  • FDA UDI c5e558ab-ebd7-4ba0-8b91-9d7f5889167c 34 fields · synced May 30, 2026