Pediguard Threaded

FDA UDI

Class II (US FDA UDI)

by Spineguard

Identity

Trade Name: PEDIGUARD THREADED FDA UDI
Generic Name: Manual surgical rotary handpiece, reusable FDA UDI
Model / Reference: DSG Threaded Shaft A LK - Ø5.5mm FDA UDI

Identifiers

Catalog Number: D1TA1001 FDA UDI
Primary DI / UDI-DI: 03662674000457 FDA UDI
FDA Product Code: PDQ FDA UDI
GMDN Term: Manual surgical rotary handpiece, reusable FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 874.1820 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

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Manual surgical rotary handpiece, reusable

Pediguard Threaded by Spineguard — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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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 II	Pending data

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Manufacturer

Manufacturer: Spineguard

Sources (1)

FDA UDI 02ab40a1-8507-47ec-9a2d-c13cbdca4e02 34 fields · synced Jun 1, 2026