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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 Dental Mouth Mirror, Simple Stem, size 8, diameter = 30 mm FDA UDI
Model / Reference
1 FDA UDI
Description
HR Dental Mouth Mirror, Simple Stem, size 8, diameter = 30 mm FDA UDI

Identifiers

Primary DI / UDI-DI
04260543224271 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
Not 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

No

FDA UDI

Röder Dentalinstrumente by Röder Dentalinstrumente GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 10fac964-4844-4997-8ee1-118e784336e6 34 fields · synced Jun 6, 2026