FDA UDI Not in Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440330650 · Model: 31271 · Neoss Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440330650
Version / Model
31271
Catalog Number
31271
Company Name
Neoss Ltd
Labeler DUNS
216693627
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-05-22
Public Version
6
Public Version Date
2021-09-20
Public Version Status
Update
Public Device Record Key
6ba23262-cc58-4333-939b-13c3795085be
Distribution End Date
2021-09-17

Device Description

Tissue Former - Narrow Incisor

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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DZE Implant, Endosseous, Root-Form

GMDN Terms

Code Name
44880 Dental implant suprastructure, temporary, preformed, single-use

Identifiers

Type ID
Primary 05060440330650

Customer Contacts

Phone
999-999-9999