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Surgical Guide - 3D Printed Model

FDA UDI

Class I (US FDA UDI)

by Institut Straumann SA

Identity

Trade Name
Surgical Guide - 3D Printed Model FDA UDI
Generic Name
Custom-made orthopaedic/craniofacial surgical guide FDA UDI
Device Name
Surgical Guide - 3D Printed Model for assistance during oral surgery. FDA UDI
Model / Reference
2017 FDA UDI
Description
Surgical Guide - 3D Printed Model for assistance during oral surgery. FDA UDI

Identifiers

Catalog Number
010.4021 FDA UDI
Primary DI / UDI-DI
07630031739933 FDA UDI
FDA Product Code
NDP FDA UDI
GMDN Term
Custom-made orthopaedic/craniofacial surgical guide 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Custom-made orthopaedic/craniofacial surgical guide

Surgical Guide - 3D Printed Model by Institut Straumann SA — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Custom-made orthopaedic/craniofacial surgical guide.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Institut Straumann SA

Sources (1)

  • FDA UDI c8f28932-0613-4b84-a3f4-63d9c852a926 35 fields · synced May 30, 2026