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Dynamic Abutment Solutions

FDA UDI

Class II (US FDA UDI)

by Talladium España Sl

Identity

Trade Name
DYNAMIC ABUTMENT SOLUTIONS FDA UDI
Generic Name
Dental precision attachment simulator/analog, reusable FDA UDI
Device Name
Dynamic Screw UNF1-72 L7.6mm 35Ncm for validation FDA UDI
Model / Reference
41.317.076.99-2 FDA UDI
Description
Dynamic Screw UNF1-72 L7.6mm 35Ncm for validation FDA UDI

Identifiers

Primary DI / UDI-DI
08435673512642 FDA UDI
FDA Product Code
NHA FDA UDI
GMDN Term
Dental precision attachment simulator/analog, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3630 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

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: Dental precision attachment simulator/analog, reusable

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

Similar devices

Also classified as Dental precision attachment simulator/analog, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Talladium España Sl

Sources (1)

  • FDA UDI ccf24f22-4004-4c3a-a644-849581147d63 35 fields · synced May 30, 2026