FDA UDI In Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440332579 · Model: 51131 · Neoss AB
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440332579
Version / Model
51131
Catalog Number
51131
Company Name
Neoss AB
Labeler DUNS
509583543
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-05
Public Version
9
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
9d350ab1-9f4b-4641-a326-8bc0af8bb5e7

Device Description

Neoss System Tray

Device Characteristics

Single Use
No
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
No
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
NDP Accessories, Implant, Dental, Endosseous

GMDN Terms

Code Name
12143 Instrument tray, reusable

Identifiers

Type ID
Primary 05060440332579

Customer Contacts

Phone
999-999-9999