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Hader

FDA UDI

Class I (US FDA UDI)

by PREAT Corporation

Identity

Trade Name
Hader FDA UDI
Generic Name
Partial denture FDA UDI
Device Name
Hader Servicing Kit (Alphadent) Kit contains: (1) Delrin Analog Bar (2) Authentic Yellow Hader Clips (2) Green Processing Spacers (1)Hader Insertion Tool (2) Traditional Metal Housings FDA UDI
Model / Reference
0101737 FDA UDI
Description
Hader Servicing Kit (Alphadent) Kit contains: (1) Delrin Analog Bar (2) Authentic Yellow Hader Clips (2) Green Processing Spacers (1)Hader Insertion Tool (2) Traditional Metal Housings FDA UDI

Identifiers

Catalog Number
0101737 FDA UDI
Primary DI / UDI-DI
00842092180211 FDA UDI
FDA Product Code
EGG FDA UDI
GMDN Term
Partial denture 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: Partial denture

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

Similar devices

Also classified as Partial denture.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
PREAT Corporation

Sources (1)

  • FDA UDI c73620af-9ef9-49da-b195-285f60f607ad 35 fields · synced Jun 1, 2026