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Kontact

FDA UDI

Class I (US FDA UDI)

by Biotech Dental

Identity

Trade Name
KONTACT FDA UDI
Generic Name
Dental implant system FDA UDI
Device Name
Pilot drill Ø2.0mm for L10mm implant for Atlasurgery system FDA UDI
Model / Reference
KATLAFE2010 FDA UDI
Description
Pilot drill Ø2.0mm for L10mm implant for Atlasurgery system FDA UDI

Identifiers

Catalog Number
KATLAFE2010 FDA UDI
Primary DI / UDI-DI
03701045243878 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implant system FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3980 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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

Yes

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
MRI Safety
MR Conditional FDA UDI

Category: Dental implant system

Kontact by Biotech Dental — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Biotech Dental

Sources (1)

  • FDA UDI 025435dc-3b3e-4a07-9ffb-dcd98ebce0d6 35 fields · synced May 30, 2026