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Rinn®

FDA UDI

Class I (US FDA UDI)

by Dentsply International

Identity

Trade Name
RINN® FDA UDI
Generic Name
Dental x-ray film holder, reusable FDA UDI
Device Name
RINN® XCP-DS FIT® Posterior Sensor Holders FDA UDI
Model / Reference
559902 FDA UDI
Description
RINN® XCP-DS FIT® Posterior Sensor Holders FDA UDI

Identifiers

Catalog Number
559902 FDA UDI
Primary DI / UDI-DI
D0035599021 FDA UDI
FDA Product Code
EGZ FDA UDI
GMDN Term
Dental x-ray film holder, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.1905 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

No

FDA UDI

Category: Dental x-ray film holder, reusable

Rinn® by Dentsply International — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental x-ray film holder, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI cf5bf218-b91a-4486-9205-b3b80f2b48e9 35 fields · synced May 30, 2026