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Protective Cap (CNC)

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref 024.2324-04

by Institut Straumann AG

Identity

Trade Name
STRAUMANN MAGELLAN(TM) ABUTMENT,PROTECTIVE CAP, COPINGS, BASAL SCREW FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
Protective Cap (CNC) EUDAMED
Protective cap for screw-retained abutment, D 3.5mm, H 6.5mm, PEEK/TAN FDA UDI
Model / Reference
024.2324-04 EUDAMED
Protective caps FDA UDI
Description
Protective cap for screw-retained abutment, D 3.5mm, H 6.5mm, PEEK/TAN FDA UDI

Identifiers

Catalog Number
024.2324-04 FDA UDI
Primary DI / UDI-DI
07630031710345 EUDAMEDFDA UDI
Basic UDI-DI
0763003170082QW EUDAMED
Unit of Use DI
07630031755926 EUDAMED
510(k) Number
K133421 FDA UDI
FDA Product Code
NHA FDA UDI
EMDN Code
P01020101 DENTAL IMPLANTS EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
872.3630 FDA UDI
Market of Registration
Germany 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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 3.5 Millimeter FDA UDI

Protective Cap (CNC) by Institut Straumann AG — Class IIa — 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

EUDAMED SRN
CH-MF-000009933
Authorised Representative
Etkon GmbH DE-AR-000009335

Sources (2)

  • EUDAMED 4a78b4c9-5fc9-4e08-ad0e-a4c9e688a74c 61 fields · synced Aug 2, 2026
  • FDA UDI d7369829-0e50-4121-a236-5c6ee2e1c98b 37 fields · synced May 30, 2026