Drill Guide 3.1mm

FDA UDI

Class I (US FDA UDI)

by Genesis Biologics, Inc.

Identity

Trade Name: DRILL GUIDE 3.1MM FDA UDI
Generic Name: Surgical drill guide, reusable FDA UDI
Device Name: DRILL GUIDE 3.1MM FDA UDI
Model / Reference: 50DG0031 FDA UDI
Description: DRILL GUIDE 3.1MM FDA UDI

Identifiers

Catalog Number: 50DG0031 FDA UDI
Primary DI / UDI-DI: 00850005827450 FDA UDI
FDA Product Code: FZX FDA UDI
GMDN Term: Surgical drill guide, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 878.4800 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size: Outer Diameter — 3.1 Millimeter FDA UDI

Category: Surgical drill guide, reusable

Drill Guide 3.1mm by Genesis Biologics, Inc. — 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: Genesis Biologics, Inc.

Sources (1)

FDA UDI 20b40a4d-8256-4da1-8e32-d5bf48f13bf9 36 fields · synced May 30, 2026