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Alliedstar Sensa

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 6583318Model AS 100, AS 200E, AS 260, AS 260a, S300W, ST 200E, ST 300E, NeoScan 1000, NeoScan 2000, Owandy ios, Owandy ios Wireless, DI-1

by Alliedstar Medical Equipment Co., Ltd.

Identity

Trade Name
Alliedstar Sensa EUDAMEDFDA UDI
Alliedstar Sensa Intraoral Scanner Advanced Demo EUDAMED
Generic Name
Intraoral optical scanning system FDA UDI
Device Name
Intraoral Scanner EUDAMED
Model / Reference
AS 100, AS 200E, AS 260, AS 260a, S300W, ST 200E, ST 300E, NeoScan 1000, NeoScan 2000, Owandy ios, Owandy ios Wireless, DI-1 EUDAMED
6583318 EUDAMED
S300W FDA UDI

Identifiers

Catalog Number
6583318 FDA UDI
Primary DI / UDI-DI
06973993442284 EUDAMEDFDA UDI
Basic UDI-DI
697399344alliedstar01SL EUDAMED
FDA Product Code
NOF FDA UDI
EMDN Code
Q010207 DENTAL IMPRESSION DEVICES FOR PROSTHETIC DENTISTRY EUDAMED
GMDN Term
Intraoral optical scanning system FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
872.3661 FDA UDI
Market of Registration
Hungary EUDAMED
Italy 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

No

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Dental implant suprastructure, temporary, preformed, single-use

Alliedstar Sensa by Alliedstar Medical Equipment Co., Ltd. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implant suprastructure, temporary, preformed, single-use.

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
CN-MF-000008845
Authorised Representative
Etkon GmbH DE-AR-000009335

Sources (3)

  • EUDAMED c35fa230-4cf8-4422-b24b-c81baff879d2 61 fields · synced Jun 18, 2026
  • FDA UDI f61762a7-973c-4049-ae4e-9d660eeb7db9 33 fields · synced May 30, 2026
  • EUDAMED 6e25819d-0ab7-4022-b0c7-631ba6035208 61 fields · synced Jun 11, 2026