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Prodont-Holliger

FDA UDI

Class I (US FDA UDI)

by Prodont-Holliger

Identity

Trade Name
PRODONT-HOLLIGER FDA UDI
Generic Name
Dental mirror, reusable FDA UDI
Device Name
micromirror css pure reflect ø5mm FDA UDI
Model / Reference
MP4305PH FDA UDI
Description
micromirror css pure reflect ø5mm FDA UDI

Identifiers

Catalog Number
MP4305PH FDA UDI
Primary DI / UDI-DI
03665224016472 FDA UDI
FDA Product Code
EAX FDA UDI
GMDN Term
Dental mirror, reusable 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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental mirror, reusable

Prodont-Holliger by Prodont-Holliger — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental mirror, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Prodont-Holliger

Sources (1)

  • FDA UDI 5de6dfad-c565-4403-bf2f-b632dc0f40f5 34 fields · synced May 30, 2026