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Dci

FDA UDI

Class I (US FDA UDI)

by DCI International, LLC

Identity

Trade Name
DCI FDA UDI
Generic Name
Dental delivery system instrument unit, pneumatic FDA UDI
Device Name
Reliance Post Mount Utilities, PMU, Gray FDA UDI
Model / Reference
RO4052 FDA UDI
Description
Reliance Post Mount Utilities, PMU, Gray FDA UDI

Identifiers

Primary DI / UDI-DI
00810021438269 FDA UDI
FDA Product Code
EIA FDA UDI
GMDN Term
Dental delivery system instrument unit, pneumatic FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.6640 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental delivery system instrument unit, pneumatic

Dci by DCI International, LLC — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental delivery system instrument unit, pneumatic.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI f02da960-7d2b-454f-b6ab-6eb53f94a5ad 34 fields · synced Jun 9, 2026