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Schick33

FDA UDI

Class II (US FDA UDI)

by Sirona Dental, Inc.

Identity

Trade Name
SCHICK33 FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Device Name
SCHICK33 S1 SENSOR SHIP KIT 6 FT FDA UDI
Model / Reference
B1118000 FDA UDI
Description
SCHICK33 S1 SENSOR SHIP KIT 6 FT FDA UDI

Identifiers

Primary DI / UDI-DI
D764B11180001 FDA UDI
510(k) Number
K093453 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

Yes

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

Schick33 by Sirona Dental, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental digital imaging sensor, intraoral.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Sirona Dental, Inc.

Sources (1)

  • FDA UDI ff662ccf-d8ee-43a3-82d7-9704d45d3f33 35 fields · synced May 30, 2026