Diamodent

FDA UDI

Class I (US FDA UDI)

by Diamodent

Identity

Trade Name: Diamodent FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Device Name: Lab Screwdriver .050" Hex White FDA UDI
Model / Reference: N/A FDA UDI
Description: Lab Screwdriver .050" Hex White FDA UDI

Identifiers

Catalog Number: T5510 FDA UDI
Primary DI / UDI-DI: D907T55100 FDA UDI
FDA Product Code: DZN FDA UDI
GMDN Term: Surgical screwdriver, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.4565 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

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Category: Surgical screwdriver, reusable

Diamodent by Diamodent — Class I — 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 I	Pending data

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Manufacturer

Manufacturer: Diamodent

Sources (1)

FDA UDI 76670055-02f1-4ea2-88e8-96afc426cee0 34 fields · synced May 30, 2026