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AlliedStar

FDA UDI

Class II (US FDA UDI)

by Alliedstar Medical Equipment Co., Ltd.

Identity

Trade Name
AlliedStar FDA UDI
Generic Name
Intraoral optical scanning system FDA UDI
Device Name
Handpiece Spare FDA UDI
Model / Reference
AS 200E FDA UDI
Description
Handpiece Spare FDA UDI

Identifiers

Catalog Number
6583217 FDA UDI
Primary DI / UDI-DI
06973993440037 FDA UDI
FDA Product Code
NOF FDA UDI
GMDN Term
Intraoral optical scanning system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.3661 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

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

No

FDA UDI

Category: Intraoral optical scanning system

AlliedStar by Alliedstar Medical Equipment Co., Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intraoral optical scanning system.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI bc811c80-b3fb-4b19-bd61-c9f3307a60f4 34 fields · synced May 30, 2026