← Back to catalogue

Caps Extr./Insertion Tool W. Udi

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 485IC-US-SIS

by Rhein 83 S.r.l.

Identity

Trade Name
CAPS EXTR./INSERTION TOOL W. UDI EUDAMED
OT EQUATOR - OT BRIDGE FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Strumenti (Regola 1) EUDAMED
STERILIZABLE device with stainless steel insertion and extraction tip for retentive caps and plastic handle FDA UDI
Model / Reference
485IC-US-SIS EUDAMED
CAPS EXTR./INSERTION TOOL W. UDI FDA UDI
Description
STERILIZABLE device with stainless steel insertion and extraction tip for retentive caps and plastic handle FDA UDI

Identifiers

Catalog Number
485IC-US-SIS FDA UDI
Primary DI / UDI-DI
08059224172477 EUDAMEDFDA UDI
Basic UDI-DI
805804571STRPB EUDAMED
Direct Marketing DI
08059224172477 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010280 PROSTHETIC DENTISTRY DEVICES - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Italy EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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

Caps Extr./Insertion Tool W. Udi by Rhein 83 S.r.l. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Rhein 83 S.r.l.
EUDAMED SRN
IT-MF-000005998

Sources (2)

  • EUDAMED 68e5eee5-a397-4ea2-812c-7e1e5d7979eb 61 fields · synced Oct 6, 2026
  • FDA UDI 1ec0cef7-b7e4-49a4-8fcf-e29fb5616d27 34 fields · synced May 27, 2026