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Preat

FDA UDI

Class I (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Preat FDA UDI
Generic Name
Root canal post kit FDA UDI
Device Name
Preci Post DDS refill. Kit contains:. 50 Yellow Opaque Impression Posts (00842092175545). 50 Blue Opaque Impression Posts (00842092175552) FDA UDI
Model / Reference
0102002 FDA UDI
Description
Preci Post DDS refill. Kit contains:. 50 Yellow Opaque Impression Posts (00842092175545). 50 Blue Opaque Impression Posts (00842092175552) FDA UDI

Identifiers

Catalog Number
0102002 FDA UDI
Primary DI / UDI-DI
00842092175576 FDA UDI
FDA Product Code
ELR FDA UDI
GMDN Term
Root canal post kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.3810 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

Category: Root canal post kit

Preat by PREAT Corporation — 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

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI 3a4b5092-b0ad-41ff-b3d6-9582097c3ad7 35 fields · synced May 30, 2026