Ceka & Preci-Line Attachments

FDA UDI

Class I (US FDA UDI)

by Alpha-Dent

Identity

Trade Name: CEKA & PRECI-LINE ATTACHMENTS FDA UDI
Generic Name: Dental mandrel FDA UDI
Device Name: PRECI-BAR MINI PARAL. MANDREL 1 P. FDA UDI
Model / Reference: 1102 P FDA UDI
Description: PRECI-BAR MINI PARAL. MANDREL 1 P. FDA UDI

Identifiers

Catalog Number: 1102 P FDA UDI
Primary DI / UDI-DI: 04260576942531 FDA UDI
FDA Product Code: EGG FDA UDI
GMDN Term: Dental mandrel FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3165 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Safe FDA UDI

Category: Dental mandrel

Ceka & Preci-Line Attachments by Alpha-Dent — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Preat — PREAT Corporation · Class I
Preat — PREAT Corporation · Class I
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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Alpha-Dent

Sources (1)

FDA UDI 816e22dc-0769-47d3-afa9-29d0f61430ad 35 fields · synced Jun 6, 2026