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Snapshot

FDA UDI

Class II (US FDA UDI)

by PaloDEx Group Oy

Identity

Trade Name
Snapshot FDA UDI
Generic Name
Dental digital imaging sensor, intraoral FDA UDI
Model / Reference
SC-I-2-S2 FDA UDI

Identifiers

Catalog Number
900167 FDA UDI
Primary DI / UDI-DI
06430035872527 FDA UDI
FDA Product Code
MUH FDA UDI
GMDN Term
Dental digital imaging sensor, intraoral FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
872.1800 FDA UDI
Commercial Distribution
Not 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

Snapshot by PaloDEx Group Oy — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PaloDEx Group Oy

Sources (1)

  • FDA UDI b0f1d5b3-643d-4483-bb5d-5a5df42751b3 35 fields · synced May 30, 2026