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Schick

FDA UDI

Class II (US FDA UDI)

by Dentsply International

Identity

Trade Name
Schick FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
SCHICK33 S0 STARTER KIT/AE INTERFACE 6FT FDA UDI
Model / Reference
100008639 FDA UDI
Description
SCHICK33 S0 STARTER KIT/AE INTERFACE 6FT FDA UDI

Identifiers

Catalog Number
100008639 FDA UDI
Primary DI / UDI-DI
D0031000086390 FDA UDI
FDA Product Code
EAP FDA UDI
MQB FDA UDI
GMDN Term
Dental digital imaging sensor, intraoral FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1810 FDA UDI
892.1680 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

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental digital imaging sensor, intraoral

Schick by Dentsply International — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 55da1b1d-75a9-4c9b-b6c1-984f0e146ae6 34 fields · synced Jun 8, 2026