Drill Tube

FDA UDI

Class I (US FDA UDI)

by POINTIMPLANT Co., Ltd.

Identity

Trade Name: Drill Tube FDA UDI
Generic Name: Surgical drill guide, reusable FDA UDI
Model / Reference: NDT20 FDA UDI

Identifiers

Primary DI / UDI-DI: 08800011265786 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Surgical drill guide, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 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

Yes

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Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

MRI Safety

MR Conditional FDA UDI

Category: Surgical drill guide, reusable

The Drill Tube is a medical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue, providing precise control and safety during dental procedures.

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Hintermann Series — Dt Medtech, LLC · 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: POINTIMPLANT Co., Ltd.

Sources (1)

FDA UDI 723459d2-c36e-4426-bf00-da677288a200 32 fields · synced Jul 14, 2026