FDA UDI Not in Commercial Distribution 🇺🇸 United States

Neoss Implant System

DI: 05060440332685 · Model: 51153 · Neoss Ltd
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Neoss Implant System
Primary DI
05060440332685
Version / Model
51153
Catalog Number
51153
Company Name
Neoss Ltd
Labeler DUNS
216693627
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-08
Public Version
5
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
5354f27d-8e54-4874-80ac-48798d68c8a1
Distribution End Date
2021-09-17

Device Description

Neoss® Guide Kit Ø3.5 - Ø4.5

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
Yes
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
45697 Fixture/appliance dental drill bit, single-use

Identifiers

Type ID
Primary 05060440332685

Customer Contacts

Phone
999-999-9999