LOCATOR ABUTMENT PRE/KOH 3.30 1671

GUDID 00840481117305

LOCATOR ABUTMENT PRE/KOH 3.30 H.2 MM

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed
Primary Device ID00840481117305
NIH Device Record Key8d456dab-23cd-4f52-ac4d-986a850bb1aa
Commercial Distribution StatusIn Commercial Distribution
Brand NameLOCATOR ABUTMENT PRE/KOH 3.30
Version Model Number1671
Catalog Number1671
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
GS100840481117305 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00840481117305]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number5
Public Version Date2019-11-08
Device Publish Date2016-08-05

On-Brand Devices [LOCATOR ABUTMENT PRE/KOH 3.30]

00840481117312LOCATOR ABUTMENT PRE/KOH 3.30 H.3 MM
00840481117305LOCATOR ABUTMENT PRE/KOH 3.30 H.2 MM
00840481117299LOCATOR ABUTMENT PRE/KOH 3.30 H.1 MM

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