FDA UDI In Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440333644 · Model: 31365 · Neoss AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440333644
Version / Model
31365
Catalog Number
31365
Company Name
Neoss AB
Labeler DUNS
509583543
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-18
Public Version
4
Public Version Date
2021-03-26
Public Version Status
Update
Public Device Record Key
af8a69cf-2e2a-42c3-b75a-15e4e7f9e726

Device Description

ScanPeg – 5 pcs

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
High-level Disinfectant

Product Codes

Code Name
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

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

Identifiers

Type ID
Primary 05060440333644

Customer Contacts

Phone
999-999-9999