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DEXcam3™ intra-oral camera sheaths

FDA UDI

Class I (US FDA UDI)

by Dexis Llc

Identity

Trade Name
DEXcam3™ intra-oral camera sheaths FDA UDI
Generic Name
Cable/lead/sensor/probe cover, sterile FDA UDI
Device Name
100 Count FDA UDI
Model / Reference
0.822.6921 FDA UDI
Description
100 Count FDA UDI

Identifiers

Catalog Number
PLU795002 FDA UDI
Primary DI / UDI-DI
EKAV082269210 FDA UDI
FDA Product Code
KQM FDA UDI
GMDN Term
Cable/lead/sensor/probe cover, sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Cable/lead/sensor/probe cover, sterile

DEXcam3™ intra-oral camera sheaths by Dexis Llc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Cable/lead/sensor/probe cover, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dexis Llc

Sources (1)

  • FDA UDI ddd91a54-c7f5-4c76-ae37-e715f5067965 36 fields · synced Jun 1, 2026