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TRANSFER PLUS CAP pz.50

EUDAMEDFDA UDI

Class I (EU MDR)

Ref CAIP-50

by Rhein 83 S.r.l.

Identity

Trade Name
TRANSFER PLUS CAP pz.50 EUDAMED
OT EQUATOR - OT BRIDGE FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
TRANSFER EUDAMED
DISPOSABLE device used to create a housing for a retentive cap inside a removable dental prosthesis FDA UDI
Model / Reference
CAIP-50 EUDAMED
TRANSFER PLUS CAP 50 pcs. FDA UDI
Description
DISPOSABLE device used to create a housing for a retentive cap inside a removable dental prosthesis FDA UDI

Identifiers

Catalog Number
CAIP-50 FDA UDI
Primary DI / UDI-DI
08059224169392 EUDAMEDFDA UDI
Basic UDI-DI
805804571TRFNJ EUDAMED
FDA Product Code
EGG FDA UDI
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3165 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

Category: Dental implant suprastructure, temporary, preformed, single-use

TRANSFER PLUS CAP pz.50 by Rhein 83 S.r.l. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

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

Sources (2)

  • EUDAMED 11d17d9a-86fa-4c51-95bc-a4f03e1b063b 61 fields · synced Jun 18, 2026
  • FDA UDI cd860687-dcb1-48ec-9955-df8cb30b4410 34 fields · synced May 29, 2026