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Disposa-Shield®

FDA UDI

Class I (US FDA UDI)

by Dentsply Professional

Identity

Trade Name
Disposa-Shield® FDA UDI
Generic Name
Cable/lead/sensor/probe cover, non-sterile FDA UDI
Device Name
Disposa-Shield® Surface Barrier For Midwest®RDH Freedom® Inner Module Trial Pack. Box of 25 FDA UDI
Model / Reference
90736 FDA UDI
Description
Disposa-Shield® Surface Barrier For Midwest®RDH Freedom® Inner Module Trial Pack. Box of 25 FDA UDI

Identifiers

Primary DI / UDI-DI
D003907361 FDA UDI
FDA Product Code
EFB FDA UDI
PEM FDA UDI
GMDN Term
Cable/lead/sensor/probe cover, non-sterile FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4200 FDA UDI
878.4370 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

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

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

Disposa-Shield® by Dentsply Professional — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 6de0be81-b312-458e-af4c-2e83db42ff5f 35 fields · synced Jun 1, 2026