FDA UDI In Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440335266 · Model: 31382 · Neoss AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440335266
Version / Model
31382
Catalog Number
31382
Company Name
Neoss AB
Labeler DUNS
509583543
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-12
Public Version
2
Public Version Date
2022-04-26
Public Version Status
Update
Public Device Record Key
8c039f7d-107f-4441-8221-045e66a0d476

Device Description

Prepable Abutment Blanks CoCr SSC, Ø12 mm, NP – 5 pc

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
NHA Abutment, Implant, Dental, Endosseous

GMDN Terms

Code Name
44879 Dental implant suprastructure, permanent, preformed

Identifiers

Type ID
Primary 05060440335266

Customer Contacts

Phone
999-999-9999