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Mguide®

FDA UDI

Class I (US FDA UDI)

by Dentsply Ih, Inc.

Identity

Trade Name
MGUIDE® FDA UDI
Generic Name
Dental implantation drilling template, custom-made FDA UDI
Device Name
MGUIDE - 4 implants FDA UDI
Model / Reference
MG-STN4 FDA UDI
Description
MGUIDE - 4 implants FDA UDI

Identifiers

Primary DI / UDI-DI
07392532253171 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Dental implantation drilling template, custom-made 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

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Dental implantation drilling template, custom-made

Mguide® by Dentsply Ih, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Dental implantation drilling template, custom-made.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Dentsply Ih, Inc.

Sources (1)

  • FDA UDI 9010e8e8-0250-41c5-8c86-1babad15025e 34 fields · synced Jun 1, 2026