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DIOnavi. Guide (Anchor system)

FDA UDI

Class I (US FDA UDI)

by DIO Corporation

Identity

Trade Name
DIOnavi. Guide (Anchor system) FDA UDI
Generic Name
Dental guided surgery reference plate FDA UDI
Model / Reference
GUIDE02 00 A01(a,b) FDA UDI

Identifiers

Primary DI / UDI-DI
08800049415696 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental guided surgery reference plate 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

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental guided surgery reference plate

DIOnavi. Guide (Anchor system) by DIO Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental guided surgery reference plate.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
DIO Corporation

Sources (1)

  • FDA UDI bb056c00-46f5-4766-b3ab-728c58578322 32 fields · synced May 31, 2026