Doctor Direct Sales (dds)

FDA UDI

Class I (US FDA UDI)

by Handpiece Parts & Repairs, Inc.

Identity

Trade Name: DOCTOR DIRECT SALES (DDS) FDA UDI
Generic Name: Dental power tool system handpiece, pneumatic FDA UDI
Device Name: DDS PRO HYGIENIST HANDPIECE FDA UDI
Model / Reference: H5600 FDA UDI
Description: DDS PRO HYGIENIST HANDPIECE FDA UDI

Identifiers

Catalog Number: H5600 FDA UDI
Primary DI / UDI-DI: 00810988030964 FDA UDI
FDA Product Code: EFB FDA UDI
GMDN Term: Dental power tool system handpiece, pneumatic FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4200 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Dental power tool system handpiece, pneumatic

Doctor Direct Sales (dds) by Handpiece Parts & Repairs, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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UltraPro Tx — ULTRADENT PRODUCTS, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Handpiece Parts & Repairs, Inc.

Sources (1)

FDA UDI 782c5df6-9398-49e7-93b3-1b036072445a 34 fields · synced Jun 1, 2026