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Hader Bar

FDA UDI

Class I (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Hader Bar FDA UDI
Generic Name
Dental impression spacer FDA UDI
Device Name
Hader Bar Master Kit (6) Plastic Bar Patterns (6) Yellow Hader Riders (6) Green Processing Spacers (6) Alignment Metal Housings (1) Hader Insertion Tool FDA UDI
Model / Reference
0101750 FDA UDI
Description
Hader Bar Master Kit (6) Plastic Bar Patterns (6) Yellow Hader Riders (6) Green Processing Spacers (6) Alignment Metal Housings (1) Hader Insertion Tool FDA UDI

Identifiers

Catalog Number
0101750 FDA UDI
Primary DI / UDI-DI
00842092105450 FDA UDI
FDA Product Code
EGG FDA UDI
GMDN Term
Dental impression spacer 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

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: Dental impression spacer

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

Similar devices

Also classified as Dental impression spacer.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI 72e7fd9d-1e79-41fa-8ef5-4c65092e4c00 35 fields · synced May 30, 2026