FDA UDI In Commercial Distribution 🇺🇸 United States

INVERTA®

DI: 06009544027362 · Model: IV-EX3512D-4513 · SOUTHERN IMPLANTS (PTY) LTD
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
INVERTA®
Primary DI
06009544027362
Version / Model
IV-EX3512D-4513
Catalog Number
IV-EX3512D-4513
Company Name
SOUTHERN IMPLANTS (PTY) LTD
Labeler DUNS
636239584
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-22
Public Version
1
Public Version Date
2021-11-30
Public Version Status
New
Public Device Record Key
b79d4efc-c05b-4e22-bf0e-92bdd9f6621b

Device Description

INVERTA®, Ø3.5 ExHex 12° CO-AXIS®, Ø4.5 x 13mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
55849 Screw endosteal dental implant, two-piece

Identifiers

Type ID
Primary 06009544027362

Premarket Submissions

Submission Number Supplement Number
K181850 000