← Back to catalogue

Dynamic Abutment Solutions

FDA UDIEUDAMED

Class I (US FDA UDI)

Ref 79.300.001.02-2Model ACCKIT04

by Talladium España Sl

Identity

Trade Name
DYNAMIC ABUTMENT SOLUTIONS FDA UDI
Generic Name
Dental prosthesis removal instrument FDA UDI
Device Name
MOUNT EXTRACTOR EUDAMED
Mount extractor M2.5 L32,00mm Hex.1.20 FDA UDI
Model / Reference
79.300.001.02-2 EUDAMEDFDA UDI
ACCKIT04 EUDAMED
Description
Mount extractor M2.5 L32,00mm Hex.1.20 FDA UDI

Identifiers

Primary DI / UDI-DI
08435673509918 EUDAMEDFDA UDI
Basic UDI-DI
843656873ACCKIT043C EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010280 PROSTHETIC DENTISTRY DEVICES - ACCESSORIES EUDAMED
GMDN Term
Dental prosthesis removal instrument FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
872.3980 FDA UDI
Market of Registration
Spain EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

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 prosthesis removal instrument

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

Similar devices

Also classified as Dental prosthesis removal instrument.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Unknown

MDR

United States Pending data

FDA UDI

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

Manufacturer

Sources (2)

  • FDA UDI f2170dd6-4e5c-4d05-8c83-d01679cc61a7 35 fields · synced Jun 18, 2026
  • EUDAMED 0eff2de8-e577-45c3-a57a-71b6bb7c62dc 61 fields · synced Jun 18, 2026