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StecoTitanmagnetics®

FDA UDI

Class I (US FDA UDI)

by steco-System-Technik GmbH & Co KG

Identity

Trade Name
StecoTitanmagnetics® FDA UDI
Generic Name
Magnetic dental precision attachment FDA UDI
Device Name
Titanmagnetics® Insert K-Line D5.2/H3.0 for Brånemark RP Implant -> For further information visit steco.de FDA UDI
Model / Reference
I.02.01.K300 FDA UDI
Description
Titanmagnetics® Insert K-Line D5.2/H3.0 for Brånemark RP Implant -> For further information visit steco.de FDA UDI

Identifiers

Catalog Number
I.02.01.K300 FDA UDI
Primary DI / UDI-DI
ESTOI0201K3000 FDA UDI
FDA Product Code
EGG FDA UDI
KCZ FDA UDI
GMDN Term
Magnetic dental precision attachment FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3165 FDA UDI
878.3800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

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
MRI Safety
MR Conditional FDA UDI

Category: Magnetic dental precision attachment

StecoTitanmagnetics® by steco-System-Technik GmbH & Co KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Magnetic dental precision attachment.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
steco-System-Technik GmbH & Co KG

Sources (1)

  • FDA UDI d434d664-e3af-4a34-99e0-7ec34977ff80 35 fields · synced May 30, 2026