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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® model analogue K-Line D5.2/H7.5 Universal -> For further information visit steco.de FDA UDI
Model / Reference
M.00.01.K750 FDA UDI
Description
Titanmagnetics® model analogue K-Line D5.2/H7.5 Universal -> For further information visit steco.de FDA UDI

Identifiers

Catalog Number
M.00.01.K750 FDA UDI
Primary DI / UDI-DI
ESTOM0001K7500 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

No

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

No

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 8d911b88-9451-4d4b-914f-c7d57de85d68 35 fields · synced Jun 1, 2026