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Preat

FDA UDI

Class I (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Preat FDA UDI
Generic Name
Resilient dental precision attachment FDA UDI
Device Name
Preci-Clix 1251 Starter Kit . kit contains . 2 Preci-Clix 1251 . 1 Clix Female Insertion Tool . 1 Preci Ball/Clix Ball Paralleling Mandrel . 1 Cup Burr FDA UDI
Model / Reference
01K1251 FDA UDI
Description
Preci-Clix 1251 Starter Kit . kit contains . 2 Preci-Clix 1251 . 1 Clix Female Insertion Tool . 1 Preci Ball/Clix Ball Paralleling Mandrel . 1 Cup Burr FDA UDI

Identifiers

Catalog Number
01K1251 FDA UDI
Primary DI / UDI-DI
00842092169230 FDA UDI
FDA Product Code
EGG FDA UDI
NDP FDA UDI
EJL FDA UDI
GMDN Term
Resilient dental precision attachment FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3165 FDA UDI
872.3980 FDA UDI
872.3240 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

Yes

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

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Resilient dental precision attachmentDental precision attachment fitting/adjustment toolDental mandrelSteel dental bur, single-use

Preat by PREAT Corporation — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Steel dental bur, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI 389bb6d7-205f-41af-abeb-458feefd088e 35 fields · synced May 30, 2026