← Back to catalogue

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
Root canal post kit FDA UDI
Device Name
PRECI-POST CC REAMER B 1 P. FDA UDI
Model / Reference
2952B FDA UDI
Description
PRECI-POST CC REAMER B 1 P. FDA UDI

Identifiers

Catalog Number
2952B FDA UDI
Primary DI / UDI-DI
04260576943231 FDA UDI
FDA Product Code
DZA FDA UDI
GMDN Term
Root canal post kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4130 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Safe FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 0.7 Millimeter FDA UDI

Category: Root canal post kit

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

Similar devices

Also classified as Root canal post kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Alpha-Dent

Sources (1)

  • FDA UDI 6e89cb21-2771-46d9-a6ce-18410d815121 36 fields · synced May 31, 2026