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Custom Ti Base Engaging Ø 5, 1 H 1.3

EUDAMEDFDA UDI

Class IIb (EU MDR)

Ref IPD/AA-IW-02/3DModel IN / INC3D / INSI

by Implant Protesis Dental 2004 S.l.

Identity

Trade Name
Custom Ti Base Engaging Ø 5,1 H 1.3 EUDAMED
IPD FDA UDI
Generic Name
Dental implant suprastructure, permanent, preformed FDA UDI
Device Name
Hollow Screw System ; Custom Interface System ; Cerec Sirona Ti Base System EUDAMED
Engaging Interface Ø 5.1 h 1.5 mm 3D FDA UDI
Model / Reference
IN / INC3D / INSI EUDAMED
IPD/AA-IW-02/3D EUDAMED
INC3D FDA UDI
Description
Engaging Interface Ø 5.1 h 1.5 mm 3D FDA UDI

Identifiers

Catalog Number
IPD/AA-IW-02/3D FDA UDI
Primary DI / UDI-DI
08435566600609 EUDAMEDFDA UDI
Basic UDI-DI
8435566603BQ EUDAMED
510(k) Number
K222215 FDA UDI
FDA Product Code
PNP FDA UDI
NHA FDA UDI
EMDN Code
Q01020602 COMBINED DENTAL PROSTHESES EUDAMED
GMDN Term
Dental implant suprastructure, permanent, preformed FDA UDI

Classification

Device Class
Class IIb EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

Sutures

Yes

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

No

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

Custom Ti Base Engaging Ø 5, 1 H 1.3 by Implant Protesis Dental 2004 S.l. — Class IIb — MDR, FDA UDI — listed in EUDAMED, FDA GUDID

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

EUDAMED SRN
ES-MF-000002195

Sources (2)

  • EUDAMED 511da0d9-9440-4bdf-9cfe-68e63e55d88b 61 fields · synced Oct 6, 2026
  • FDA UDI 7bf6fa0d-ea62-49bb-988e-0fc96f2443be 36 fields · synced May 30, 2026