STRAIGHT PRE-MADE ABUTMENT A-MD-TS-330-30

GUDID D7701441153

STRAIGHT PRE-MADE ABUTMENT D.3.30, H.3 MM

SWEDEN & MARTINA SPA

Dental implant suprastructure, permanent, preformed
Primary Device IDD7701441153
NIH Device Record Key2edab575-dcc3-4682-bf76-3bf1cd68c65f
Commercial Distribution StatusIn Commercial Distribution
Brand NameSTRAIGHT PRE-MADE ABUTMENT
Version Model NumberA-MD-TS-330-30
Catalog NumberA-MD-TS-330-30
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
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com
Phone844.862.7846
Emailinfo.us@sweden-martina.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCD7701441153 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NHAAbutment, Implant, Dental, Endosseous

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

[D7701441153]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-11-03
Device Publish Date2020-10-26

On-Brand Devices [STRAIGHT PRE-MADE ABUTMENT]

D7701107053STRAIGHT PRE-MADE ABUTMENT H3 HEX 2,50 MM, PRE-KOH
D7701107023STRAIGHT PRE-MADE ABUTMENT H3 HEX 2,30 MM, PRE-KOH
D7701096083STRAIGHT PRE-MADE ABUTMENT H5 HEX 2,50 MM, PRE-KOH
D7701096073STRAIGHT PRE-MADE ABUTMENT H2 HEX 2,50 MM, PRE-KOH
D7701096063STRAIGHT PRE-MADE ABUTMENT H1 HEX 2,50 MM, PRE-KOH
D7701096053STRAIGHT PRE-MADE ABUTMENT H0,5 HEX 2,50 MM, PRE-KOH
D7701096033STRAIGHT PRE-MADE ABUTMENT H5 HEX 2,30 MM, PRE-KOH
D7701096023STRAIGHT PRE-MADE ABUTMENT H2 HEX 2,30 MM, PRE-KOH
D7701096013STRAIGHT PRE-MADE ABUTMENT H1 HEX 2,30 MM, PRE-KOH
D7701096003STRAIGHT PRE-MADE ABUTMENT H0,5 HEX 2,30 MM, PRE-KOH
D7701441183STRAIGHT PRE-MADE ABUTMENT D.3.80, H.3 MM
D7701441173STRAIGHT PRE-MADE ABUTMENT D.3.80, H.2 MM
D7701441163STRAIGHT PRE-MADE ABUTMENT D.3.80, H.1 MM
D7701441153STRAIGHT PRE-MADE ABUTMENT D.3.30, H.3 MM
D7701441143STRAIGHT PRE-MADE ABUTMENT D.3.30, H.2 MM
D7701441133STRAIGHT PRE-MADE ABUTMENT D.3.30, H.1 MM
D7701441123STRAIGHT PRE-MADE ABUTMENT D.3.30, H.0,5 MM
D7701605183STRAIGHT PRE-MADE ABUTMENT D.3,80, H.15MM, REPOSITIONABLE
D7701605173STRAIGHT PRE-MADE ABUTMENT D.3,30, H.15MM, REPOSITIONABLE
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.