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Dynamic Abutment Solutions

FDA UDI

Class I (US FDA UDI)

by Talladium España Sl

Identity

Trade Name
DYNAMIC ABUTMENT SOLUTIONS FDA UDI
Generic Name
Steel dental bur, reusable FDA UDI
Device Name
Guided drill Ø2.5mm L10 FDA UDI
Model / Reference
74.100.225.01-2 FDA UDI
Description
Guided drill Ø2.5mm L10 FDA UDI

Identifiers

Primary DI / UDI-DI
08435673507136 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Steel dental bur, reusable 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

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

Yes

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

Category: Steel dental bur, reusable

Dynamic Abutment Solutions by Talladium España Sl — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Steel dental bur, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7e1a43e2-0912-45f2-b7f6-711c8540691f 35 fields · synced May 31, 2026