MILLABLE POST, REP., INTERNAL A-TG-MFI-W

GUDID D7700874793

MILLABLE POST, REP., INTERNAL PROF., PRE-KOH TG, WIDE PLAT.

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed
Primary Device IDD7700874793
NIH Device Record Key7cee9dbe-3bdf-4872-a310-ab746aee9fbb
Commercial Distribution StatusIn Commercial Distribution
Brand NameMILLABLE POST, REP., INTERNAL
Version Model NumberA-TG-MFI-W
Catalog NumberA-TG-MFI-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
HIBCCD7700874793 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[D7700874793]

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 [MILLABLE POST, REP., INTERNAL]

D7700874793MILLABLE POST, REP., INTERNAL PROF., PRE-KOH TG, WIDE PLAT.
D7700874783MILLABLE POST, REP., INTERNAL PROF., PRE-KOH TG, MEDIUM PLAT.

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.