Screwdriver Bit Torx

FDA UDI

Class I (US FDA UDI)

by Neurovention LLC

Identity

Trade Name: Screwdriver Bit Torx FDA UDI
Generic Name: Surgical screwdriver, single-use, non-sterile FDA UDI
Device Name: Screwdriver Bit T4 Torx, Single Use FDA UDI
Model / Reference: 333-01 FDA UDI
Description: Screwdriver Bit T4 Torx, Single Use FDA UDI

Identifiers

Primary DI / UDI-DI: G28433301 FDA UDI
FDA Product Code: HAO FDA UDI
GMDN Term: Surgical screwdriver, single-use, non-sterile FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 882.4535 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

Yes

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

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: Surgical screwdriver, single-use, non-sterile

Screwdriver Bit Torx by Neurovention LLC — 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: Neurovention LLC

Sources (1)

FDA UDI 33db953b-29d8-437f-a52b-7f71ada2a868 33 fields · synced Jun 8, 2026