SCREW M2 FOR RIP.ABUTMENT A-TG-VABUR-W

GUDID D7700884153

SCREW M2 FOR RIP.ABUTMENT PRE-KOH TG, WIDE, MAGENTA

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed
Primary Device IDD7700884153
NIH Device Record Keycbde99ee-3f51-4bae-8513-ddb3a9b3f263
Commercial Distribution StatusIn Commercial Distribution
Brand NameSCREW M2 FOR RIP.ABUTMENT
Version Model NumberA-TG-VABUR-W
Catalog NumberA-TG-VABUR-W
Company DUNS433815198
Company NameSWEDEN & MARTINA SPA
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone844.862.7846
Emailinfo.us@sweden-martina.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD7700884153 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[D7700884153]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2015-10-01

On-Brand Devices [SCREW M2 FOR RIP.ABUTMENT]

D7700886153SCREW M2 FOR RIP.ABUTMENT PRE-KOH TG,WIDE,MAGENTA(10PCS)
D7700884153SCREW M2 FOR RIP.ABUTMENT PRE-KOH TG, WIDE, MAGENTA

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