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DIA-300i

FDA UDI

Class I (US FDA UDI)

by DiaDent Group International

Identity

Trade Name
DIA-300i FDA UDI
Generic Name
Face splash shield, reusable FDA UDI
Device Name
Dia-300i goggles protects eyes from flying debris and harmful substances. It is most effective in preventing eye injuries and contamination from fine dust FDA UDI
Model / Reference
- FDA UDI
Description
Dia-300i goggles protects eyes from flying debris and harmful substances. It is most effective in preventing eye injuries and contamination from fine dust FDA UDI

Identifiers

Catalog Number
1005-1041 FDA UDI
Primary DI / UDI-DI
08806383500401 FDA UDI
FDA Product Code
HOY FDA UDI
GMDN Term
Face splash shield, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.4750 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

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

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Face splash shield, reusable

DIA-300i by DiaDent Group International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Face splash shield, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 07108832-e325-4a98-ba3e-c68cd43fa48e 35 fields · synced Jun 1, 2026