← Back to catalogue

Dental Accessory

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 260-100-860

by Bicon, LLC

Identity

Trade Name
UA Temporization Sleeve FDA UDI
Generic Name
Dental implant suprastructure, temporary, preformed, single-use FDA UDI
Device Name
Dental Accessory EUDAMED
UA6 LP Temporization Sleeves (3) FDA UDI
Model / Reference
260-100-860 EUDAMEDFDA UDI
Description
UA6 LP Temporization Sleeves (3) FDA UDI

Identifiers

Catalog Number
260-100-860 FDA UDI
Primary DI / UDI-DI
00813110027078 EUDAMEDFDA UDI
Basic UDI-DI
B-00813110027078 EUDAMED
081311002ACC42 EUDAMED
FDA Product Code
NDP FDA UDI
EMDN Code
Q010280 PROSTHETIC DENTISTRY DEVICES - ACCESSORIES EUDAMED
GMDN Term
Dental implant suprastructure, temporary, preformed, single-use FDA UDI

Classification

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

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

Yes

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

Dental Accessory by Bicon, Llc — Class I — MDD, MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Bicon, LLC
EUDAMED SRN
US-MF-000002782
Authorised Representative
Bicon Europe Ltd IE-AR-000002497

Sources (3)

  • EUDAMED 51512658-2881-4e96-ba0a-81fda40360d4 61 fields · synced Jul 9, 2026
  • EUDAMED 7042cbfb-5199-4f09-a84e-05073fdce4a6 61 fields · synced May 16, 2026
  • FDA UDI c3103cc5-a8bc-416a-9f0a-cc617200db03 35 fields · synced May 30, 2026