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Dental Equipments

FDA UDI

Class I (US FDA UDI)

by Rhein 83 Srl

Identity

Trade Name
DENTAL EQUIPMENTS FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
DISPOSABLE device used to contain the retentive cap inside the removable prosthesis. FDA UDI
Model / Reference
S/STEEL HOUSING STANDARD size 100 u. FDA UDI
Description
DISPOSABLE device used to contain the retentive cap inside the removable prosthesis. FDA UDI

Identifiers

Catalog Number
CA011-100 FDA UDI
Primary DI / UDI-DI
08059224129860 FDA UDI
FDA Product Code
EGG FDA UDI
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3165 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

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 implant suprastructure, permanent, preformed

Dental Equipments by Rhein 83 Srl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, permanent, preformed.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Rhein 83 Srl

Sources (1)

  • FDA UDI 381b3f8f-636e-4c98-bb2d-32dcdab912bb 34 fields · synced Jun 6, 2026