‘MagnaCap’ Magnetic Retention System

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref LAA1

by Technovent Limited

Identity

Trade Name: Mini Lab Analogue Abutment EUDAMED
‘MagnaCap’ Magnetic Retention System FDA UDI
Generic Name: Magnetic dental precision attachment FDA UDI
Device Name: 'MagnaCap' Magnetic Retention System EUDAMED
The Technovent Magnacap System is a magnetic attachment system for implant retained craniofacial and dental prostheses. FDA UDI
Model / Reference: LAA1 EUDAMED
Magnacap Mini Lab Analogue Abutment FDA UDI
Description: The Technovent Magnacap System is a magnetic attachment system for implant retained craniofacial and dental prostheses. FDA UDI

Identifiers

Catalog Number: LAA1 FDA UDI
Primary DI / UDI-DI: 05060483010939 EUDAMEDFDA UDI
Basic UDI-DI: 506048301TF5DD EUDAMED
Direct Marketing DI: 05060483010939 EUDAMED
FDA Product Code: EGG FDA UDI
EMDN Code: Y0699 EXTERNAL PROSTHESES AND ORTHOSES - OTHER EUDAMED
GMDN Term: Magnetic dental precision attachment FDA UDI

Classification

Device Class: Class I EUDAMEDFDA UDI
Regulation Number: 872.3165 FDA UDI
Market of Registration: Malta EUDAMED
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

EUDAMEDFDA UDI

Single Use

Yes

FDA UDI

Implantable

EUDAMEDFDA UDI

Reusable

EUDAMED

Contains Latex

EUDAMEDFDA UDI

Reprocessed

EUDAMED

CMR Substance

EUDAMED

Human-derived

EUDAMED

Human Tissues

EUDAMED

Animal Tissues

EUDAMED

Endocrine Disruptor

EUDAMED

Administering Medicine

EUDAMED

Measuring Function

EUDAMED

Incorporates Medicinal Product

EUDAMED

Prescription Use

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

MRI Safety

MR Unsafe FDA UDI

Category: Magnetic dental precision attachment

‘MagnaCap’ Magnetic Retention System by Technovent Limited — Class I — MDR, FDA UDI — listed in FDA GUDID, EUDAMED — regulatory data on deviCERTS

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Also classified as Magnetic dental precision attachment.

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Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
EUDAMED	European Union	MDR	—	Class I	Unknown
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Technovent Limited

Sources (2)

FDA UDI b7b48255-50c5-4e5c-89dc-4fa84654baa0 35 fields · synced Jun 19, 2026
EUDAMED 508a9c1d-e6a3-4076-8c56-57581a6031b2 61 fields · synced Jun 19, 2026