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Röder Dentalinstrumente

FDA UDI

Class I (US FDA UDI)

by Röder Dentalinstrumente GmbH & Co. KG

Identity

Trade Name
Röder Dentalinstrumente FDA UDI
Generic Name
Dental mirror, reusable FDA UDI
Device Name
HR Front Dental Mouth Mirror, Cone Socket, size 6, diameter =26 mm FDA UDI
Model / Reference
1 FDA UDI
Description
HR Front Dental Mouth Mirror, Cone Socket, size 6, diameter =26 mm FDA UDI

Identifiers

Primary DI / UDI-DI
04260543220068 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

Röder Dentalinstrumente by Röder Dentalinstrumente GmbH & Co. KG — 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

Sources (1)

  • FDA UDI 2a4b1f6d-2f7c-4df5-864b-d0d3efe8622d 33 fields · synced May 30, 2026