Surgical Guide

GUDID 06972677870108

Endosseous dental implant accessories.

Modern Dental Laboratory (DG) Co., Ltd.

Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic surgical guide, non-sterile Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide Custom-made orthopaedic/craniofacial surgical guide

Primary Device ID	06972677870108
NIH Device Record Key	2338ed38-f721-4de0-a2b1-0c85005f28b5
Commercial Distribution Status	In Commercial Distribution
Brand Name	Surgical Guide
Version Model Number	010
Company DUNS	551746187
Company Name	Modern Dental Laboratory (DG) Co., Ltd.
Device Count	1
DM Exempt	true
Pre-market Exempt	true
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	true
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06972677870108 [Primary]

FDA Product Code

NDP	Accessories, Implant, Dental, Endosseous