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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
Telescoping Arm Assistants Instrum. Premium 4 Position Precision Comfort (Syr, 2 HVE, SE) Anodized FDA UDI
Model / Reference
5485 FDA UDI
Description
Telescoping Arm Assistants Instrum. Premium 4 Position Precision Comfort (Syr, 2 HVE, SE) Anodized FDA UDI

Identifiers

Primary DI / UDI-DI
00810021434629 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 54a31fb0-d98b-4383-9526-13f543819bc5 34 fields · synced Jun 9, 2026